Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 241
Acrysol EL 135, Product Information Sheet, Corel Pharma, India, 2013.
Acrysol K 140, Product Information Sheet, Corel Pharma, India, 2013.
Aerosil 200, Product Information Sheet, Gangwal Chemicals Ltd, India, 2013.
Agrawal AG, Kumar A, Gide PS. Self emulsifying drug delivery system for enhanced
solubility and dissolution of glipizide. Colloids and Surfaces B: Biointerfsaces, 2015;
126: 553-560.
Agrawal S, Chauhan S, Mathur R. Antifertility effects of embelin in male rats.
Andrologia, 1986; 18 (2): 125-131.
Ahuja BK, Jena SK, Paidi SK, Bagri S, Suresh S. Formulation, optimization and in-
vitro–in-vivo evaluation of febuxostat nanosuspension. International Journal of
Pharmaceutics, 2015; 478: 540-552.
Akhter MH, Ahmad A, Ali J. Formulation and Development of CoQ10-Loaded S-
SNEDDS for Enhancement of Oral Bioavailability. Journal of Pharmaceutical
Innovation, 2014; 9: 121-131.
Akinlade B, Elkordy AA, Essa EA, Elhagar S. Liquisolid systems to improve the
dissolution of furosemide. Scientia Pharmaceutica, 2010; 78 (2): 325-344.
Ali HS, York P, Ali AM, Blagden N. Hydrocortisone nanosuspensions for ophthalmic
delivery: A comparative study between microfluidic nanoprecipitation and wet
milling. Journal of Controlled Release, 2011; 149 (2): 175-181.
Ambrus R, Kocbek P, Kristl J, Sibanc R, Rajko R, Szabo-Revesz P. Investigation of
preparation parameters to improve the dissolution of poorly water-soluble meloxicam.
International Journal of Pharmaceutics, 2009; 381: 153-159.
Anton N, Vandamme TF. Nano-emulsions and micro-emulsions: clarifications of the
critical differences. Pharmaceutical Research, 2011; 28(5): 978-985.
Aungst GJ. Intestinal permeation enhancers. Journal of Pharmaceutical Sciences,
2000; 89(4): 429-442.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 242
Avachat AM, Patel VG. Self nanoemulsifying drug delivery system of stabilized
ellagic acid–phospholipid complex with improved dissolution and permeability. Saudi
Pharmaceutical Journal, 2015; 23 (3): 276-289.
Azeem A, Rizwan M, Ahmad FJ, Iqbal Z, Khar RK, Aqil M, Talegaonkar S.
Nanoemulsion components screening and selection: A Technical Note. AAPs
PharmSciTech, 2009; 10 (1): 69-76.
Badawy MA, Kamel AO, Sammour OA. Use of biorelevant media for assessment of a
poorly soluble weakly basic drug in the form of liquisolid compacts: in-vitro and in-
vivo study. Drug Delivery, 2016; 23 (3): 818-827.
Baek IH, Kim JS, Ha ES, Choo GH, Cho W, Hwang SJ, Kim MS. Dissolution and
oral absorption of pranlukast nanosuspensions stabilized by hydroxypropylmethyl
cellulose. International Journal of Biological Macromolecules, 2014; 67: 53-57.
Balakrishnan P, Lee BJ, Oh DH, Kim JO, Hong MJ, Jee JP, Kim JA, Yoo BK, Woo
JS, Yong CS, Choi HG. Enhanced oral bioavailability of dexibuprofen by a novel
solid self-emulsifying drug delivery system (SEDDS). European Journal of
Pharmaceutics and Biopharmaceutics, 2009; 72 (3): 539-545.
Bandivadekar MM, Pancholi SS, Kaul-Ghanekar R, Choudhari A, Koppikar S. Self-
microemulsifying smaller molecular volume oil (Capmul MCM) using non-ionic
surfactants: a delivery system for poorly water-soluble drug. Drug Development and
Industrial Pharmacy, 2012; 38 (7): 883-892.
Bandyopadhyay S, Katare OP, Singh B. Optimized self nano-emulsifying systems of
ezetimibe with enhanced bioavailability potential using long chain and medium chain
triglycerides. Colloids Surface B: Biointerfaces, 2012; 100: 50-61.
Banker GS. Tablets. In: Lachman L. Liberman HA. The Theory and Practice of
Industrial Pharmacy, 3rd ed. Varghese Publishing House. 1987: 293-345.
Basa S, Muniyappan T, Karatgi P, Prabhu R, Pillai R. Production and in-vitro
characterization of solid dosage form incorporating drug nanoparticles. Drug
Development and Industrial Pharmacy, 2008; 34 (11): 1209-1218.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 243
Basalious EB, Shawky N, Badr-Eldin SM. SNEDDS containing bioenhancers for
improvement of dissolution and oral absorption of lacidipine. I: Development and
optimization. International Journal of Pharmaceutics, 2010; 391: 203-211.
Benet LZ, Cummins CL. The drug efflux-metabolism alliance: biochemical aspects.
Advanced Drug Delivery Reviews, 2001; 50(1): S3-11.
Bhakay A, Merwade M, Bilgili E, Dave RN. Novel aspects of wet milling for the
production of microsuspensions and nanosuspensions of poorly water-soluble drugs.
Drug Development and Industrial Pharmacy, 2011; 37 (8): 963-976.
Biradar SV, Dhumal RS, Paradkar AR. Rheological investigation of self-
emulsification process: effect of co-surfactant. Journal of Pharmacy and
Pharmaceutical Sciences, 2009; 12 (2): 164-174.
Blagden N, Matas M, Gavan PT, York P. Crystal engineering of active
pharmaceutical ingredients to improve solubility and dissolution rates. Advanced
Drug Delivery Reviews, 2007; 59: 617-630.
Bolton S. Optimization techniques in pharmaceutical statistics: practical and clinical
applications. New York: Marcel Dekker, Inc.; 1997.
Borhade VB, Nair HA, Hegde DD. Development and characterization of self-
microemulsifying drug delivery system of tacrolimus for intravenous administration.
Drug Development and Industrial Pharmacy, 2009; 35: 619-630.
Bose S, Schenck D, Ghosh I, Hollywood A, Maulit E, Ruegger C. Application of
spray granulation for conversion of a nanosuspension into a dry powder form.
European Journal of Pharmaceutical Sciences, 2012; 47: 35-43.
Brahmankar DM, Jaiswal BS. Biopharmaceutics and Pharmacokinetics, A treatise. 1st
ed. Vallabh Prakashan, New Delhi, 1987.
Brij 35, Product Information Sheet, Sisco Research Lab, India, 2013.
Burra S, Yamsani M, Vobalaboina V. The liquisolid technique: an overview.
Brazilian Journal of Pharmaceutical Sciences, 2011; 47 (3): 475-482.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 244
Cab-O-Sil® M-5, Product Information Sheet, Sigma Aldrich, India, 2013.
Capryol 90, Product Information Sheet, Gattefosse Pvt Ltd, India, 2013.
Carr RL. Evaluating flow properties of solids. Chemical Engineering, 1965; 72: 163-
168.
Cerdeira AM, Mazzotti M, Gander B. Miconazole nanosuspensions: Influence of
formulation variables on particle size reduction and physical stability. International
Journal of Pharmaceutics, 2010; 396 (1-2): 210-218.
Cerdeira AM, Werner IA, Mazzotti M, Gander B. Simultaneous quantification of
polymeric and surface active stabilizers of nanosuspensions by using near-infrared
spectroscopy. Drug Development and Industrial Pharmacy, 2012; 38(11): 1360-1370.
Cerpnjak K, Zvonar A, Vrecer F, Gasperlin M. Development of a solid self-
microemulsifying drug delivery system (SMEDDS) for solubility enhancement of
naproxen. Drug Development and Industrial Pharmacy, 2015; 41 (9): 1548-1557.
Chakraborty S, Shukla D, Mishra B, Singh S. Lipid-An emerging platform for oral
delivery of drugs with poor bioavailability. European Journal of Pharmaceutics and
Biopharmaceutics, 2009; 73:1-15.
Challa R, Ahuja A, Ali J, Khar RK. Cyclodextrins in Drug Delivery: An Updated
Review. AAPS PharmSciTech, 2005; 6 (2) Article 43: E329-E357.
Chambin O, Karbowiak T, Djebili L, Jannin V, Champion D, Pourcelot Y, Cayot P.
Influence of drug polarity upon the solid-state structure and release properties of self-
emulsifying drug delivery systems in relation with water affinity. Colloids and
Surfaces B: Biointerfaces, 2009; 71(1): 73-78.
Chan HK, Kwok PC. Production methods for nanodrug particles using the bottom up
approach. Advanced Drug Delivery Reviews, 2011; 63: 406-416.
Chan LW, Lee CC, Heng PW. Ultrafine grinding using a fluidized bed opposed jet
mill effects of feed load and rotational speed of classifier wheel on particle shape.
Drug Development and Industrial Pharmacy, 2002; 28: 939-947.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 245
Chen M, Lipid excipients and delivery systems for pharmaceutical development: A
regulatory perspective, Advanced Drug Delivery Reviews, 2008; 60: 768-777.
Chen X, Matteucci ME, Lo CY, Johnston KP, Williams RO III. Flocculation of
polymer stabilized nanocrystal suspensions to produce redispersible powders. Drug
Development and Industrial Pharmacy, 2009; 35 (3): 283-296.
Chhabra G, Chuttani K, Mishra AK, Pathak K. Design and development of
nanoemulsion drug delivery system of amlodipine besilate for improvement of oral
bioavailability. Drug Development and Industrial Pharmacy, 2011; 37 (8): 907-916.
Chitra M, Shyamala C, Sukumar E. Antibacterial activity of embelin. Fitoterapia,
2003; 74: 401-403.
Choi J, Yoo JY, Kwak H, Nam BU, Lee J. Role of polymeric stabilizers for drug
nanocrystal dispersions. Current Applied Physics, 2005; 5: 472-474.
Choi MJ, Briancon S, Andrieu J, Min SG, Fessi H. Effect of freeze drying process
conditions on the stability of nanoparticles. Drying Technology: An International
Journal, 2004; 22 (1-2): 335-346.
Constantinides PP, Scalart J. Formulation and physical characterization of water in oil
microemulsion containing long versus medium chain glycerides. International
Journal of Pharmaceutics, 1997; 158: 57-68.
Constantinides PP. Lipid microemulsions for improving drug dissolution and oral
absorption: physical and biopharmaceutical aspects. Pharmaceutical Research, 1995;
12(11): 1561-72.
Costa FO, Sousa JJS, Pais AACC, Formosinho SJ. Comparison of dissolution profiles
of Ibuprofen pellets. Journal of Controlled Release, 2003; 89: 199-212.
Costa P, Lobo JM. Modeling and comparison of dissolution profiles. European
Journal of Pharmaceutical Sciences, 2001; 13 (2): 123-33.
Cremophor RH 40, Product Information Sheet, BASF, India, 2013.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 246
Crisp MT, Tucker CJ, Rogers TL, Williams III RO, Johnston KP. Turbidimetric
measurement and prediction of dissolution rates of poorly soluble drug nanocrystals.
Journal of Controlled Release, 2007; 117: 351-359.
Cui J, Yu B, Zhao Y, Zhu W, Li H, Lou H, Zhai G. Enhancement of oral absorption
of curcumin by self-microemulsifying drug delivery systems. International Journal of
Pharmaceutics, 2009; 371: 148-155.
Dai X, Moffat JG, Wood J, Reading M. Thermal scanning probe microscopy in the
development of pharmaceuticals. Advanced Drug Delivery Reviews, 2012; 64 (5):
449-60.
Das S, Suresh PK. Nanosuspension: a new vehicle for the improvement of the
delivery of drugs to the ocular surface. Application to amphotericin B. Nanomedicine:
Nanotechnology, Biology, and Medicine, 2011; 7: 242-247.
Date AA, Nagarsenker MS. Design and evaluation of self nanoemulsified drug
delivery systems (SNEDDS) for Cefpodoxime Proxetil. International Journal of
Pharmaceutics, 2007; 329: 166-172.
Date AA, Patravale VB. Current strategies for engineering drug nanoparticles.
Current Opinion in Colloid & Interface Science, 2004; 9: 222– 235.
Dejaegher B, Vander HY. Experimental designs and their recent advances in set up
data interpretation and analytical applications. Journal of Pharmaceutical and
Biomedical Analysis, 2011; 56: 141-158.
Deng J, Huang L, Liu F. Understanding the structure and stability of paclitaxel
nanocrystals. International Journal of Pharmaceutics, 2010; 390 (2): 242-249.
Desai PP, Date AA, Patravale VB. Overcoming poor oral bioavailability using
nanoparticle formulations – opportunities and limitations. Drug Discovery Today:
Technologies, 2012; 9(2): 87-95.
Deshmukh A, Kulkarni S. Solid self-microemulsifying drug delivery system of
ritonavir. Drug Development and Industrial Pharmacy, 2014; 40 (4): 477-487.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 247
Detroja C, Chavhan S, Sawant K. Enhanced Antihypertensive Activity of Candesartan
Cilexetil Nanosuspension: Formulation, Characterization and Pharmacodynamic
Study. Scientia Pharmaceutica, 2011; 79 (3): 635-651.
Dhami N. Trends in Pharmacognosy: A modern science of natural medicines. Journal
of Herbal Medicine, 2013; 3(4): 123-131.
Ditner C, Bravo R, Imanidis G, Kuentz M. A systematic dilution study of self-
microemulsifying drug delivery systems in artificial intestinal fluid using dynamic
laser light backscattering. Drug Development and Industrial Pharmacy, 2009; 35 (2):
199-208.
Dixit AR, Rajput SJ, Patel SG. Preparation and bioavailability assessment of
SMEDDS containing valsartan. AAPS PharmSciTech, 2010; 11 (1): 314-321.
Dixit RP, Nagarsenker MS. Self-nanoemulsifying granules of ezetimibe: Design,
optimization and evaluation. European Journal of Pharmaceutical Sciences, 2008;
35: 183-192.
Dolenc A, Kristil J, Baumgartner S, Planinsek O. Advantages of celecoxib
nanosuspension formulation and transformation into tablets. International Journal of
Pharmaceutics, 2009; 376: 204-212.
Dressman JB, Amidon GL, Reppas C, Shah VP. Dissolution testing as a prognostic
tool for oral drug absorption: immediate release dosage forms. Pharmaceutical
Research, 1998; 15(1): 11-22.
El-Badry M, Haq N, Fetih G, Shakeel F. Solubility and dissolution enhancement of
tadalafil using self-nanoemulsifying drug delivery system. Journal of Oleo Science,
2014; 63 (6): 567-576.
Elkordy AA, Essa EA, Dhuppad S, Jammigumpula P. Liquisolid technique to enhance
and to sustain griseofulvin dissolution: effect of choice of non-volatile liquid vehicles.
International Journal of Pharmaceutics, 2012; 434 (1-2): 122-132.
Elkordy AA, Tan XN, Essa EA. Spironolactone release from liquisolid formulations
prepared with Capryol™ 90, Solutol® HS-15 and Kollicoat® SR 30 D as non-volatile
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 248
liquid vehicles. European Journal of Pharmaceutics and Biopharmaceutics, 2013; 83
(2): 203-223.
Elnaggar YSR, El-Massik MA, Abdallah OY. Self-nanoemulsifying drug delivery
systems of tamoxifen citrate: Design and optimization. International Journal of
Pharmaceutics, 2009; 380 (1-2): 133-141.
Emad BB, Nevine S, Shaimaa MB. SNEDDS containing bioenhancers for
improvement of dissolution and oral absorption of lacidipine. I: Development and
optimization. International Journal of Pharmaceutics, 2010; 391: 203-211.
Fahmy RH, Kassem MA. Enhancement of famotidine dissolution rate through
liquisolid tablets. Formulation. In-vitro and in-vivo evaluation. European Journal of
Pharmaceutics and Biopharmaceutics, 2008; 69: 993-1003.
Fakes MG, Vakkalagadda BJ, Qian F, Desikan S, Gandhi RB, Lai C, Hsieh
A, Franchini MK, Toale H, Brown J. Enhancement of oral bioavailability of an HIV-
attachment inhibitor by nanosizing and amorphous formulation approaches.
International Journal Pharmaceutics, 2009; 370 (1-2): 167-174.
Farrokhpay S. A review of polymeric dispersant stabilisation of titania pigment.
Advances in Colloid Interface Science, 2009; 151 (1-2): 24-32.
FDA guidance for industry: Bioanalytical method validation. US Department of
Health and Human Services, Food and Drug Administration, Centre for Drug
Evaluation and Research, 2001.
Feng G, Haijun Z, Jing H, Baogang X, Fen L, Helin X, Minmin L, Chunlian X. Self
microemulsifying drug delivery system for improved oral bioavailability of
dipyridamole: preparation and evaluation. Archives of Pharmaceutical Research,
2011; 34 (7): 1113-1123.
Fricker G, Kromp T, Wendel A, Blume A, Zirkel J, Rebmann H, Setzer C, Quinket
RO, Martin F, Muller-Goymann C. Phospholipids and lipid based formulations in oral
drug delivery. Pharmaceutical Research, 2010; 27 (8): 1469-1486.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 249
Gabrielsson J, Nyström A, Lundstedt T. Multivariate methods in developing an
evolutionary strategy for tablet formulation. Drug Development and Industrial
Pharmacy, 2000; 26 (3): 275-96.
Gadhave MV, Banerjee SK. Preparation and characterization of spherical crystals of
embelin to improve the solubility and micromeritic properties. International Journal
of Pharmaceutical and Clinical Research, 2014; 6 (4): 363-369.
Gahoi S, Jain GK, Tripathi R, Pandey SK, Anwar M, Warsi MH, Singhal M, Khar
RK, Ahmad FJ. Enhanced antimalarial activity of lumefantrine nanopowder prepared
by wet-milling DYNO MILL technique. Colloids and Surfaces B:
Biointerfaces, 2012; 95: 16-22.
Ganta S, Paxton JW, Baguley BC, Garg S. Formulation and pharmacokinetic
evaluation of an asulacrine nanocrystalline suspension for intravenous delivery.
International Journal of Pharmaceutics, 2009; 367 (1-2): 179-186.
Gao L, Zhang D, Chen M, Zheng T, Wang S. Preparation and characterization of an
oridonin nanosuspension for solubility and dissolution velocity enhancement. Drug
Development and Industrial Pharmacy, 2007; 33: 1332-1339.
Gao L, Zhang D, Chenb M, Duana C, Dai W, Jia L, Zhaoa W. Studies on
pharmacokinetics and tissue distribution of oridonin nanosuspensions. International
Journal of Pharmaceutics, 2008; 355: 321-327.
Gao L, Liu G, Ma J, Wang X, Zhou L, Li X. Drug nanocrystals: In-vivo
performances. Journal of Controlled Release, 2012; 160(3): 418-430.
Gao Y, Li Z, Sun M, Guo C, Yu A, Xi Y, Cui J, Lou H, Zhai G. Preparation and
characterization of intravenously injectable curcumin nanosuspension. Drug Delivery,
2011; 18 (2): 131-142.
Gao Y, Wang Y, Ma Y, Yu A, Cai F, Shao W, Zhai G. Formulation optimization and
in situ absorption in rat intestinal tract of quercetin-loaded microemulsion. Colloids
and Surfaces B: Biointerfaces, 2009; 71: 306-314.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 250
Garala K, Patel J, Patel A, Dharamsi A. Enhanced encapsulation of metoprolol tartrate
with carbon nanotubes as adsorbent. Applied Nanoscience, 2011; 1: 219-230.
Gelucire 44/14, Product Information Sheet, Gattefosse Pvt Ltd, India, 2013.
Gershanik T, Benita S. Self-dispersing lipid formulations for improving oral
absorption oflipophilic drugs. European Journal of Pharmaceutics and
Biopharmaceutics, 2000; 50: 179-188.
Ghosh I, Bose S, Vippagunta R, Harmon F. Nanosuspension for improving the
bioavailability of a poorly soluble drug and screening of stabilizing agents to inhibit
crystal growth. International Journal of Pharmaceutics, 2011; 409 (1-2): 260-268.
Ghosh MN. Fundamentals of experimental pharmacology, 3rd ed. SK Ghosh and
Others, Calcutta, India, 2008.
Ghosh PK, Murthy RSR. Microemulsions: A Potential Drug Delivery System.
Current Drug Delivery, 2006; 3: 167-180.
GIA report analysis, 2012 http://www.nutraceuticalsworld.com/contents/view_
breaking-news/2012-03-07/global-herbal-supplement-market-to-reach-107-billion-by-
2017 (Accessed on 20/02/14).
Giliyar C, Fikstad DT, Tyavanagimatt S. Challenges and opportunities in oral delivery
of poorly water-soluble drugs. Drug Delivery Technology, 2006; 6: 57-63.
Gubbi SR, Jarag R. Formulation and characterization of atorvastatin calcium
liquisolid compacts. Asian Journal of Pharmaceutical Sciences, 2010; 5 (2): 50-60.
Guo B, Zhong S, Li N, Li X, Yi J, Jin M. Dissolution enhancement of cefdinir with
hydroxypropyl-β-cyclodextrin. Drug Development and Industrial Pharmacy, 2013;
39(11): 1638-1643.
Guo Y, Wang Y, Xu L. Enhanced bioavailability of rebamipide nanocrystal tablets:
Formulation and in-vitro/in-vivo evaluation. Asian Journal of Pharmaceutical
Sciences, 2015; 10: 223-229.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 251
Gupta R, Sharma AK, Sharma MC, Gupta RS. Antioxidant activity and protection of
pancreatic β-cells by embelin in streptozotocin-induced diabetes. Journal of Diabetes,
2012; 4: 248-256.
Gupta S, Chavhan S, Sawant KK. Self-nanoemulsifying drug delivery system for
adefovir dipivoxil: Design, characterization, in-vitro and ex vivo evaluation. Colloids
and Surfaces A: Physicochemical and Engineering Aspects, 2011; 392: 145-155.
Gupta S, Kesarla R, Omri A. Formulation Strategies to Improve the Bioavailability of
Poorly Absorbed Drugs with Special Emphasis on Self-Emulsifying Systems. ISRN
Pharmaceutics, 2013; Article ID 848043.
Gursoy RN, Benita S. Self-emulsifying drug delivery systems for improved oral
delivery of lipophilic drugs. Biomedicine and Pharmacotherapy, 2004; 58:173-182.
Han S, Yao T, Zhang X, Gan L, Zhu C, Yu H, Gan Y. Lipid based formulations to
enhance oral bioavailability of the poorly water soluble drug anethol trithione: Effect
of lipid composition and formulation. International Journal of Pharmaceutics, 2009;
379: 18-24.
Harrar A, Zech O, Klaus A, Bauduin P, Kunz W. Influence of surfactant
amphiphilicity on the phase behavior of IL-based microemulsions. Journal of Colloid
and Interface Science, 2011; 362: 423–429.
Hauss DJ. Oral lipid based formulations. Advanced Drug Delivery Reviews, 2007; 59:
667-676.
Haware RV, Tho I, Bauer-Brandl A. Application of multivariate methods to
compression behavior evaluation of directly compressible materials. European
Journal of Pharmaceutics and Biopharmaceutics, 2009; 72 (1): 148-55.
He CX, He ZG, Gao JQ. Microemulsions as drug delivery systems to improve the
solubility and the bioavailability of poorly water soluble drugs. Expert Opinion on
Drug Delivery, 2010; 7: 445-460.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 252
Hentzschel CM, Alnaief M, Smirnova I, Sakmann A, Leopold CS. Enhancement of
griseofulvin release from liquisolid compacts. European Journal of Pharmaceutics
and Biopharmaceutics, 2012; 80 (1): 130-135.
Holm R, Porter CJH, Mullertz A. Structured triglyceride vehicles for oral delivery of
halofantrine examination of intestinal lymphatic transport and bioavailability in
conscious rats. Journal of Pharmaceutical Research, 2002; 19: 1354-1361.
Horter D, Dressman JB. Influence of physicochemical properties on dissolution of
drugs in the gastrointestinal tract. Advanced Drug Delivery Reviews, 2001; 46: 75-87.
Hou C, Wang J, Le Y, Zou H, Zhao H. Preparation of azithromycin nanosuspensions
by reactive precipitation method. Drug Development and Industrial Pharmacy, 2012;
38 (7): 848-854.
https://pubchem.ncbi.nlm.nih.gov/compound/embelin (Accessed on 05/02/2013).
Huang Y, Luo X, You X, Xia Y, Song X, Yu L. The preparation and evaluation of
water-soluble SKLB610 nanosuspensions with improved bioavailability. AAPS
PharmSciTech, 2013;14 (3): 1236-1243.
Hussein A, El-Menshawe S, Afouna M. Enhancement of the in-vitro dissolution and
in-vivo oral bioavailability of silymarin from liquid-filled hard gelatin capsules of
semisolid dispersion using Gelucire 44/14 as a carrier. Pharmazie, 2012; 67 (3): 209-
214.
ICH Harmonized tripartite guideline validation of analytical procedures: text and
methodology Q2 (R1), Parent Guideline dated October 27, 1994 (complementary
guideline on methodology dated November 6, 1996 incorporated in November 2005).
Indian Pharmacopoeia (IP); The controller of Publication: New Delhi, 2014.
Jackson CL, McKenna GB. The melting behaviour of organic materials confined in
porous solids. The Journal of Chemical Physics, 1990; 93 (12): 9002-9011.
Jakki R, Afzal Syed M, Kandadi P, Veerabrahma K. Development of a self-
microemulsifying drug delivery system of domperidone: In-vitro and in-vivo
characterization. Acta Pharmaceutica, 2013; 63 (2): 241-251.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 253
Jannin V, Musakhanian J, Marchaud D. Approaches for the development of solid and
semi-solid lipid-based formulations. Advanced Drug Delivery Reviews, 2008; 60(6):
734-746.
Javadzadeh Y, Jafari-Navimipour B, Nokhodchi A. Liquisolid technique for
dissolution rate enhancement of a high dose water-insoluble drug (carbamazepine).
International Journal of Pharmaceutics, 2007; 341: 26-34.
Javadzadeh Y, Shariati H, Movahhed-Danesh E, Nokhodchi A. Effect of some
commercial grades of microcrystalline cellulose on flowability, compressibility and
dissolution profile of piroxicam liquisolid compacts. Drug Development and
Industrial Pharmacy, 2009; 35: 243-251.
Jia L, Wong H, Cerna C, Weitman SD. Effect of nanonization on absorption of
301029: ex vivo and in-vivo pharmacokinetic correlations determined by liquid
chromatography/mass spectrometry. Pharmaceutical Research, 2002; 19 (8): 1091-
1096.
Joshi V, Dwivedi S, Ward GH. Increase in the specific surface area of budesonide
during storage postmicronization. Pharmaceutical Research, 2002; 19 (1): 7-12.
Joy B, Lakshmi S. Antiproliferative Properties of Embelia Ribes. The Open Process
Chemistry Journal, 2010; 3: 17-22.
Jun HK, Dong HO, Yu-Kyoung O, Chul SY, Han-Gon C. Effects of solid carriers on
the crystalline properties, dissolution and bioavailability of flurbiprofen is solid self-
nanosemulsifying drug delivery system (solid SNEDDS). European Journal of
Pharmaceutics and Biopharmaceutics, 2012; 80: 289-297.
Junghanns JAH, Müller RH. Nanocrystal technology, drug delivery and clinical
applications. International Journal of Nanomedicine, 2008; 3(3): 295-310.
Junyaprasert VB, Morakul B. Nanocrystals for enhacement of oral bioavailability for
poorly water-soluble drugs. Asian Journal of Pharmaceutical Sciences, 2015; 10: 13-
23.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 254
Kadam VD, Gattani SG. Development of colon targeted multiparticulate pulsatile
drug delivery system for treating nocturnal asthma. Drug Delivery, 2010; 17 (5): 343-
351.
Kakran M, Sahoo NG, Li L. Dissolution enhancement of quercetin through
nanofabrication, complexation, and solid dispersion. Colloids and Surfaces B:
Biointerfaces, 2011; 1: 121-130.
Kakran M, Sahoo NG, Li L, Judeh Z, Wang Y, Chong K, Loh L. Fabrication of drug
nanoparticles by evaporative precipitation of nanosuspension. International Journal
of Pharmaceutics, 2010; 383(1-2): 285-292.
Kakran M, Shegokar R, Sahoo NG, Gohla S, Li L, Müller RH. Long-term stability of
quercetin nanocrystals prepared by different methods. Journal of Pharmacy and
Pharmacology, 2012; 64 (10): 1394-1402.
Kalepu S, Manthina M, Padavala V. Oral lipid-based drug delivery systems – an
overview. Acta Pharmaceutica Sinica B, 2013; 3 (6): 361-372.
Kalhapure RS, Akamanchi KG. Oleic acid based heterolipid synthesis,
characterization and application in self-microemulsifying drug delivery system.
International Journal of Pharmaceutics, 2012; 425 (1-2): 9-18.
Kallakunta VR, Bandari S, Jukanti R, Veerareddy PR. Oral self emulsifying powder
of lercanidipine hydrochloride: Formulation and evaluation. Powder Technology,
2012; 221: 375-382.
Kamel R, Basha M. Preparation and in-vitro evaluation of rutin nanostructured
liquisolid delivery system. Bulletin of Faculty of Pharmacy, 2013; 51: 261-272.
Kang JH, Oh DH, Oh YK, Yong CS, Choi HG. Effects of solid carriers on the
crystalline properties, dissolution and bioavailability of flurbiprofen in solid self-
nanoemulsifying drug delivery system (solid SNEDDS). European Journal of
Pharmaceutics and Biopharmaceutics, 2012; 80: 289-297.
Kang MJ, Jung SY, Song WH, Park JS, Choi SU, Oh KT, Choi HK, Choi YW, Lee
J, Lee BJ, Chi SC. Immediate release of ibuprofen from Fujicalin®-based fast-
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 255
dissolving self-emulsifying tablets. Drug Development and Industrial
Pharmacy, 2011; 37 (11): 1298-1305.
Kang MJ, Kim HS, Jeon HS, Park JH, Lee BS, Ahn BK, Moon KY, Choi YW. In situ
intestinal permeability and in-vivo absorption characteristics of olmesartan
medoxomil in self-microemulsifying drug delivery system. Drug Development and
Industrial Pharmacy, 2012a; 38 (5): 587-596.
Kaparthi S, Sathesh PR. Risperidone liquisolid compacts-Formulation and evaluation.
Der Pharmacia Sinica, 2015; 6 (6): 9-15.
Karmarkar AB, Gonjari ID, Hosmani AH, Dhabale PN. Evaluation of in-vitro
dissolution profile comparison methods of sustained release tramadol hydrochloride
liquisolid compact formulations with marketed sustained release tablets. Drug
Discoveries & Therapeutics, 2010; 4 (1): 26-32.
Karmarkar AB, Gonjari ID, Hosmani AH. Liquisolid technology for dissolution rate
enhancement or sustained release. Expert Opinion Drug Delivery, 2010a; 7 (10):
1227-1234.
Kassem MA, Abdel Rahman AA, Ghorab MM, Ahmed MB, Khalil RM.
Nanosuspension as an ophthalmic delivery system for certain glucocorticoid drugs.
International Journal of Pharmaceutics, 2007; 340 (1-2): 126-133.
Kaul G, Huang J, Chatlapalli R, Ghosh K, Nagi A. Quality-by-design case study:
investigation of the role of poloxamer in immediate-release tablets by experimental
design and multivariate data analysis. AAPS PharmSciTech, 2011; 12 (4): 1064-76.
Kayaert P, Van den Mooter G. Is the amorphous fraction of a dried nanosuspension
caused by milling or by drying? A case study with Naproxen and Cinnarizine.
European Journal of Pharmaceutics and Biopharmaceutics, 2012; 81 (3): 650-656.
Kesisoglou F, Panmai S, Wu Y. Nanosizing - Oral formulation development and
biopharmaceutical evaluation. Advanced Drug Delivery Reviews, 2007; 59: 631-644.
Khadka P , Ro J, Kim H, Kim I, Kim JT, Kim H, Cho JM, Yun G, Lee J.
Pharmaceutical particle technologies: An approach to improve drug solubility,
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 256
dissolution and bioavailability. Asian Journal of Pharmaceutical Sciences, 2014; 9:
304-316.
Khan A, Iqbal Z, Shah Y, Ahmad L, Ullah Z, Ullah A. Enhancement of dissolution
rate of class II drugs (Hydrochlorthiazide); a comparative study of the two novel
approaches; solid dispersion and liquid-solid techniques. Saudi Pharmaceutical
Journal, 2015; 23: 650-657.
Khanfar M, Salem MS, Hawari R. Formulation factors affecting the release of
ezetimibe from different liquisolid compacts. Pharmaceutical Development and
Technology, 2013; 18 (2): 417-427.
Khoo SM, Humberstone AJ, Porter CJH, Edwards GA, Charman WN. Formulation
design and bioavailability assessment of lipidic self-emulsifying formulation of
halofantrine, International Journal of Pharmaceutics, 1998; 167: 155-164.
Kim CJ. Surface chemistry and colloids, Advanced pharmaceutics: physicochemical
principles, Boca Raton, FL: CRC Press, 2004; 193-256.
Kim DW, Kang JH, Oh DH, Yong CS, Choi HG. Development of novel flurbiprofen-
loaded solid self-microemulsifying drug delivery system using gelatin as solid carrier.
Journal of Microencapsulation, 2012; 29(4): 323-330.
Kim GG, Poudel BK, Marasini M, Lee DW, Hiep TT, Yang KY, Kim JO, Yong CS,
Choi HG. Enhancement of oral bioavailability of fenofibrate by solid self-
microemulsifying drug delivery systems. Drug Development and Industrial
Pharmacy, 2013; 39 (9): 1431-1438.
Kim SC, Kim DW, Shim YH, Bang JS, Oh HS, Wan Kim S, Seo MH. In-vivo
evaluation of polymeric micellar paclitaxel formulation: toxicity and efficacy. Journal
of Controlled Release, 2001; 72(1-3): 191-202.
Kimura M, Shizuki M, Miyoshi K, Sakai T, Hidaka H, Takamura H, Matoba T.
Relationship between the Molecular Structures and Emulsification Properties of
Edible Oils. Bioscience, Biotechnology, and Biochemistry, 1994; 58(7): 1258-1261.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 257
Kohli K, Chopra S, Dhar D, Arora S, Khar RK. Self-emulsifying drug delivery
systems: an approach to enhance oral bioavailability. Drug Discovery Today, 2010;
15(21-22): 958-965.
Kommavarapu P, Maruthapillai A, Palanisamy K, Sunkara M. Preparation and
characterization of rilpivirine solid dispersions with the application of enhanced
solubility and dissolution rate. Beni-Suef University Journal of Basic and Applied
Sciences, 2015; 4(1): 71-79.
Kommuru T, Gurley B, Khan M, Reddy IK. Self-emulsifying drug delivery systems
(SEDDS) of coenzyme Q10: formulation development and bioavailability assessment.
International Journal of Pharmaceutics, 2001; 212 (2): 233-246.
Kubista M, Sjogreen B, Forootan A, Sindelka R, Jonak J, Andrade JM. Real-time
PCR gene expression profiling. European Pharmaceutical Reviews, 2007; 1: 56-60.
Kuentz M, Cavegn M. Critical concentrations in the dilution of oral self-
microemulsifying drug delivery systems. Drug Development and Industrial
Pharmacy, 2010; 36 (5): 531-538.
Kulkarni AS, Aloorkar NH, Mane MS, Gaja JB. Liquiosolid sysyem:A Review.
International Journal of Pharmaceutical Sciences and Nanotechnology, 2010; 3(1):
795-802.
Kumar P, Mittal KL (eds). Handbook of Microemulsion Science and Technology,
Marshal Dekker, New York, 1999.
Labrafil M2125 CS, Product Information Sheet, Gattefosse Pvt Ltd, India, 2013.
Labrasol, Product Information Sheet, BASF, India, 2013.
Lai F, Sinico C, Ennas G, Marongiu F, Marongiu G, Fadda AM. Diclofenac
nanosuspensions: influence of preparation procedure and crystal form on drug
dissolution behaviour. International Journal of Pharmaceutics, 2009; 373 (1-2): 124-
132.
Lawrence MJ, Rees GD. Microemulsion based media as novel drug delivery systems
Advanced Drug Delivery Reviews, 2000; 45: 89-121.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 258
Leclercq SY, dos Santos RM, Macedo LB, Campos PC, Ferreira TC, de Almeida
JG, Seniuk JG, Serakides R, Silva-Cunha A, Fialho SL. Evaluation of water-in-oil-in-
water multiple emulsion and microemulsion as potential adjuvants for immunization
with rabies antigen. European Journal of Pharmaceutical Sciences, 2011; 43(5): 378-
385.
Lee J, Choi JY, Park CH. Characteristics of polymers enabling nano-comminution of
water-insoluble drugs. International Journal of Pharmaceutics, 2008; 355 (1-2): 328-
336.
Lee J. Drug nano and microparticles processed into solid dosage forms: physical
properties. Journal of Pharmaceutical Sciences, 2003; 92 (10): 2057-2068.
Lenhardt T, Vergnault G, Grenier P, Scherer D, Langguth P. Evaluation of
nanosuspensions for absorption enhancement of poorly soluble drugs: in-vitro
transport studies across intestinal epithelial monolayers. The AAPS Journal, 2008;
10(3): 435-438.
Leonard ST, Droege M. The uses and benefits of cluster analysis in pharmacy
research. Research in Social Administrative Pharmacy, 2008; 4 (1): 1-11.
Li W, Yi S, Wang Z, Chen S, Xin S, Xie J, Zhao C. Self-nanoemulsifying drug
delivery system of persimmon leaf extract: Optimization and bioavailability studies.
International Journal of Pharmaceutics, 2011; 420: 161-171.
Li W, Yang Y, Tian Y, Xu X, Chen Y, Mu L, Zhang Y, Fang L. Preparation and in-
vitro/in-vivo evaluation of revaprazan hydrochloride nanosuspension. International
Journal of Pharmaceutics, 2011a; 408 (1-2): 157-162.
Li X, Gu L, Xu Y, Wang Y. Preparation of fenofibrate nanosuspension and study of
its pharmacokinetic behavior in rats. Drug Development and Industrial
Pharmacy, 2009; 35 (7): 827-833.
Lindmark T, Nikkila T, Artursson P. Mechanism of absorption enhancement by
medium chain fatty acids in intestinal epithelial Caco-2 monolayers. The Journal of
Pharmacology and Experimental Therapeutics, 1995; 275: 958-964.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 259
Lionberger RA, Lee SL, Lee L, Raw A, Yu LX. Quality by Design: Concepts for
ANDAs. The AAPS Journal, 2008; 10 (2): 268-276.
Lipinski CA, Lombardo F, Dominy BW, Feeney PJ. Experimental and computational
approaches to estimate solubility and permeability in drug discovery and development
settings. Advance Drug Delivery Reviews, 2001; 46: 3-26.
Liu H, Shang K, Liu W, Leng D, Li R, Kong Y, Zhang T. Improved oral
bioavailability of glyburide by a self-nanoemulsifying drug delivery system. Journal
of Microencapsulation, 2014; 31(3): 277-283.
Liu P, Rong X, Laru J, van Veen B, Kiesvaara J, Hirvonen J, Laaksonen T, Peltonen
L. Nanosuspensions of poorly soluble drugs: preparation and development by wet
milling. International Journal of Pharmaceutics, 2011; 411: 215-222.
Liversidge GG, Cundy KC, Bishop J. Surface modified drug nanoparticles. US Patent
5,145,684; 1992.
Liversidge GG, Cundy KC. Particle size reduction for improvement of oral
bioavailability of hydrophobic drugs: I. Absolute oral bioavailability of
nanocrystalline danazol in beagle dogs. International Journal of Pharmaceutics,
1995; 125: 91-97.
Loh ZH, Samanta AK, Heng PWS. Overview of milling techniques for improving the
solubility of poorly water-soluble drugs. Asian Journal of Pharmaceutical Sciences,
2015; 10: 255-274.
Mahmoud EA, Bendas ER, Mohamed MI. Preparation and evaluation of self-
nanoemulsifying tablets of carvedilol. AAPS PharmSciTech, 2009; 10 (1): 183-192.
Manach C, Scalbert A, Morand C, Re´me´sy C, Jime´nez L. Polyphenols: food
sources and bioavailability. The American Journal of Clinical Nutrition, 2004; 79:
727-747.
Mariajancyrani J, Chandramohan G, Ravikumar R. Isolation and identification of
phytoconstituents from Delonic Regia Leaves. International Journal of Pharmacy and
Pharmaceutical Sciences, 2013; 5(4): 671-674.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 260
Martin A. Physical Pharmacy, 4th ed. Philadelphia. Lippincott Williams & Wilkins;
1993.
Massart DL, Heyden YV. From Tables to Visuals: Principal Component Analysis,
Part 2. LC-GC Europe, 2005; 18 (2): 84-89.
Matteucci ME, Brettmann BK, Rogers TL, Elder EJ, Williams RO 3rd, Johnston KP.
Design of potent amorphous drug nanoparticles for rapid generation of highly
supersaturated media. Molecular Pharmaceutics, 2007; 4(5): 782-793.
Mauludin R, Müller RH, Keck CM. Development of an oral rutin nanocrystal
formulation. International Journal of Pharmaceutics, 2009; 370: 202-209.
Maurya DP, Sultana Y, Aqil M, Panda BP, Ali A. Formulation and optimization of
alkaline extracted ispaghula husk microscopic reservoirs of isoniazid by box-behnken
statistical design. Journal of Dispersion Science and Technology, 2011; 32: 424-432.
Mennini N, Furlanetto S, Cirri M, Mura P. Quality by design approach for developing
chitosan Ca-alginate microspheres for colon delivery of celecoxib hydroxpropyl β-
cyclodextrin PVP complex. European Journal of Pharmaceutics and
Biopharmaceutics, 2012; 80: 67-75.
Mennini N, Furlanetto S, Maestrelli F, Pinzauti S, Mura P. Response surface
methodology in the optimization of chitosan–Ca pectinate bead formulations.
European Journal of Pharmaceutical Sciences, 2008; 35: 318-325.
Merisko-Liversidge E, Liversidge GG. Nanosizing for oral and parenteral drug
delivery: a perspective on formulating poorly-water soluble compounds using wet
media milling technology. Advanced Drug Delivery Reviews, 2011; 63(6): 427-440.
Mezghrani O, Ke X, Bourkaib N, Xu BH. Optimized self-microemulsifying drug
delivery systems (SMEDDS) for enhanced oral bioavailability of astibilin. Pharmazie,
2011; 66: 754-760.
Mohd AB, Sanka K, Bandi S, Diwan PV, Shastri N. Solid self-nanoemulsifying drug
delivery system (S-SNEDDS) for oral delivery of glimepiride: development and
antidiabetic activity in albino rabbits. Drug Delivery, 2015; 22 (4): 499-508.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 261
Monteiro A, Afolabi A, Bilgili E. Continuous production of drug nanoparticle
suspensions via wet stirred media milling: a fresh look at the Rehbinder effect. Drug
Development and Industrial Pharmacy, 2013; 39 (2): 266-283.
Mosharraf C, Nystrom C. The effect of particle size and shape on the surface specific
dissolution rate of micronized practically insoluble drugs. International Journal of
Pharmaceutics, 1995; 122: 35-47.
Mukherjee T, Plakogiannis FM. Development and oral bioavailability assessment of a
supersaturated self-microemulsifying drug delivery system (SMEDDS) of
albendazole. Journal of Pharmacy and Pharmacology, 2010; 62 (9): 1112-1120.
Muller RH, Jacobs C. Production and characterization of a budenoside
nanosuspesnion for pulmonary administration. Pharmaceutical Research, 2002; 19:
189-194.
Muller RH, Moschwitzer J, Bushrab FN. Manufacturing of nanoparticles by milling
and homogenisation techniques, In: Gupta RB, Kompella UB (ed.), Nanoparticle
Technology for Drug Delivery, Taylor and Francis Group, New York; 2006: 21-52.
Müller RH, Gohla S, Keck CM. State of the art of nanocrystals--special features,
production, nanotoxicology aspects and intracellular delivery. European Journal of
Pharmaceutics and Biopharmaceutics, 2011; 78(1): 1-9.
Müller RH, Jacobs C, Kayser O. Nanosuspensions as particulate drug formulations in
therapy. Rationale for development and what we can expect for the future. Advanced
Drug Delivery Reviews, 2001; 47 (1): 3-19.
Naik SR, Niture NT, Ansari AA, Shah PD. Anti diabetic activity of embelin:
Involvement of cellular inflammatory mediators, oxidative stress and other markers.
Phytomedicine, 2013; 20 (10): 797-204.
Nakarani M, Misra AK, Patel JK, Vaghani SS. Itraconazole nanosuspension for oral
delivery: Formulation, characterization and in-vitro comparison with marketed
formulation. Daru Journal of Faculty of Pharmacy, 2010; 18 (2): 84-90.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 262
Nanjwade BK, Patel DJ, Udhani RA, Manvi FV. Functions of lipids for enhancement
of oral bioavailability of poorly water soluble drugs. Scientia Pharmaceutica, 2011;
79(4): 705-727.
Naveen C, Shastri N, Tadikonda RR. Use of the liquisolid compact technique for
improvement of the dissolution rate of valsartan. Acta Pharmaceutica Sinica B, 2012;
2 (5): 502-508.
Nazzal S, Zaghloul AA, Khan MA. Effect of extra granular microcrystalline cellulose
on compaction, surface roughness and in-vitro dissolution of a self nanoemulsified
solid dosage form of Ubiquinone. Pharmaceutical Technology, 2002; 26: 86-98.
Nazzal S, Khan MA. Controlled release of a self-emulsifying formulation from a
tablet dosage form: stability assessment and optimization of some processing
parameters. International Journal of Pharmaceutics, 2006; 315 (1-2): 110-121.
Nekkanti V, Karatgi P, Prabhu R, Pillai R. Solid self-microemulsifying formulation
for candesartan cilexetil. AAPS PharmSciTech, 2010; 11 (1): 9-17.
Nekkanti V, Pillai R, Venkateshwarlu V, Harisudhan T. Development and
characterization of solid oral dosage form incorporating candesartan nanoparticles.
Pharmaceutical Development and Technology, 2009; 14 (3): 290-298.
Nepal PR, Han HK, Choi HK. Preparation and in-vitro-in-vivo evaluation of
Witepsol® H35 based self-nanoemulsifying drug delivery systems (SNEDDS) of
coenzyme Q10. European Journal of Pharmaceutical Sciences, 2010; 39: 224-232.
Neusilin US2, Product Information Sheet, Gangwal Chemicals Ltd, India, 2013.
Newton JM, Pinto MR, Podczeck F. The preparation of pellets containing a surfactant
or a mixture of mono- and di-gylcerides by extrusion/spheronization. European
Journal of Pharmaceutical Sciences, 2007; 30(3-4): 333-342.
Nikolovska-Coleska Z, Xu L, Hu Z, Tomita Y, Li P, Roller PP, Wang R, Fang
X, Guo R, Zhang M, Lippman ME, Yang D, Wang S. Discovery of embelin as a cell-
permeable, small-molecular weight inhibitor of XIAP through structure-based
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 263
computational screening of a traditional herbal medicine three-dimensional structure
database. Journal of Medicinal Chemistry, 2004; 47(10): 2430-2440.
Niwa T, Miura S, Danjo K. Universal wet-milling technique to prepare oral
nanosuspension focused on discovery and preclinical animal studies - Development of
particle design method. International Journal of Pharmaceutics, 2011; 405 (1-2):
218-227.
Noyes A, Whitney W. The rate of solution of solid substances in their own solutions.
Journal of American Chemical Society, 1987; 19: 930-934.
Obitte NC, Ofokansi KC, Nzekwe IF, Esimone CO, Okoye IE. Self-Nanoemulsfiying
drug delivery systems based on melon oil and its admixture with a homolipid from
Bos Indicus for the delivery of Indomethacin. Tropical Journal of Pharmaceutical
Research, 2011; 10: 299-307.
Owen MR, Armitage M, Chatfield M, Davies B, Emiabata-Smith D, Freeman Hayes
D, Mann J, Ramsay T, Smith L, Squires B. A scientist’s viewpoint on promoting
effective use of experimental design: Then things a scientist wants to know about
experimental design. Pharmaceutical Statistics, 2003; 2: 15-29.
Paceol, Product Information Sheet, Gattefosse Pvt Ltd, India, 2013.
Pandya VM, Patel JK, Patel DJ. Formulation and optimization of nanosuspensions for
enhancing simvastatin dissolution using central composite design. Dissolution
Technologies, 2011; 18 (3): 40-45.
Parmar N, Singla N, Amin S, Kohli K. Study of cosurfactant effect on
nanoemulsifying area and development of lercanidipine loaded (SNEDDS) self
nanoemulsifying drug delivery system. Colloids Surfaces B: Biointerfaces, 2011; 86
(2): 327-338.
Parveen R, Baboota S, Ali J, Ahuja A, Vasudev SS, Ahmad S. Oil based nanocarrier
for improved oral delivery of silymarin: In-vitro and in-vivo studies. International
Journal of Pharmaceutics, 2011; 413 (1-2): 245-253.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 264
Patel A, Shelat P, Lalwani A. Development and optimization of solid self-
nanoemulsifying drug delivery system (S-SNEDDS) using Scheffe’s design for
improvement of oral bioavailability of nelfinavir mesylate. Drug Delivery and
Translational Research, 2014; 4: 171-186.
Patel D, Sawant KK. Oral bioavailability enhancement of acyclovir by self-
microemulsifying drug delivery systems (SMEDDS). Drug Development and
Industrial Pharmacy, 2007; 33: 1318-1326.
Patel GV, Patel VB, Pathak A, Rajput SJ. Nanosuspension of efavirenz for improved
oral bioavailability: formulation optimization, in-vitro, in situ and in-vivo evaluation.
Drug Development and Industrial Pharmacy, 2013; 40 (1): 80-91.
Patel J, Dhingani A, Garala K, Raval M, Sheth N. Design and development of solid
nanoparticulate dosage forms of telmisartan for bioavailability enhancement by
integration of experimental design and principal component analysis. Powder
Technology, 2014a; 258: 331-343.
Patel M, Patel N, Patel R, et al. Formulation and evaluation of self-emulsifying drug
delivery system of lovastatin. Asian Journal of Pharmaceutical Sciences, 2010; 5:
266-275.
Patel RB, Patel MR, Bhatt KK, Patel BG. Formulation and characterization of
microemulsion drug delivery system for trasnasal administration of carbamazepine.
Bulletin of Faculty of Pharmacy, Cairo University, 2013a; 51 (2): 243-253.
Patel RK, Pundarikakshudu K, Momin M, Patel MM. Studies on formulation and in-
vitro dissolution of embelin tablets. Indian Journal of Pharmaceutical Sciences, 2006;
68 (2): 227-230.
Patel T, Patel LD, Suhagia BN, Soni T, Patel T. Formulation of Fenofibrate Liquisolid
Tablets Using Central Composite Design. Current Drug Delivery, 2014b; 11: 11-23.
Pathan R, Bhandari U. Preparation and characterization of embelin-phospholipid
complex as effective drug delivery tool. Journal of Inclusion Phenomena and
Macrocyclic Chemistry, 2011; 69: 139-147.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 265
Patravale VB, Date AA, Kulkarni RM. Nanosuspensions: a promising drug delivery
strategy. Journal of Pharmacy and Pharmacology, 2004; 56: 827-840.
Pavia DL. Introduction to Spectroscopy. Cengage Learning, 2009.
Poloxamer 188, Product Information Sheet, Torrent Pharmaceuticals ltd, India, 2013
Poloxamer 407, Product Information Sheet, Torrent Pharmaceuticals ltd, India, 2013
Poojari R. Embelin - a drug of antiquity: shifting the paradigm towards modern
medicine. Expert Opinion on Investigational Drugs, 2014; 23(3): 427-444.
Porter CJ, Pouton CW, Cuine JF, Charman WN. Enhancing intestinal drug
solubilisation using lipid-based delivery systems. Advanced Drug Delivery Reviews,
2008; 60 (6): 673-691.
Porter CJ, Charman WN. In-vitro assessment of oral lipid based formulations.
Advanced Drug Delivery Reviews, 2001; 50: S127–S147.
Pouton CW, Porter CJ. Formulation of lipid-based delivery systems for oral
administration: materials, methods and strategies. Advanced Drug Delivery Reviews,
2008; 60 (6): 625-637.
Pouton CW. Formulation of poorly water-soluble drugs for oral administration:
physicochemical and physiological issues and the lipid formulation classification
system. European Journal of Pharmaceutical Sciences, 2006; 29: 278-287.
Pouton CW. Lipid formulations for oral administration of drugs non emulsifying, self
emulsifying and ‘self-microemulsifying’ drug delivery systems. European Journal of
Pharmaceutics, 2000; 11 (2): 93-98.
Prajapati ST, Bulchandani HH, Patel DM, Dumaniya SK, Patel CN. Formulation and
Evaluation of Liquisolid Compacts for Olmesartan Medoxomil. Journal of Drug
Delivery, 2013; Article ID 870579: 1-9.
Pu X, Sun J, Wang Y, Wang Y, Liu X, Zhang P, Tang X, Pan W, Han J, He Z.
Development of a chemically stable 10-hydroxycamptothecin nanosuspensions.
International Journal of Pharmaceutics, 2009; 379 (1): 167-173.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 266
Pund S, Shete Y, Jagadale S. Multivariate analysis of physicochemical characteristics
of lipid based nanoemulsifying cilostazol—Quality by design. Colloids and Surfaces
B: Biointerfaces, 2014; 115: 29-36.
Rabinow BE. Nanosuspensions in drug delivery. Nature Reviews. Drug
Discovery, 2004; 3(9): 785-796.
Radfar M, Sudarshana MS, Kavitha HU, Satish S, Niranjan MH. Evaluation of
antibacterial and antifungal activity of root and root callus extracts of Trianthema
decandra L. African Journal of Biotechnology, 2012; 11(2): 510-515.
Ragonese R, Macka M, Hughes J, Petocz P. The use of the Box-Behnken
experimental design in the optimisation and robustness testing of a capillary
electrophoresis method for the analysis of ethambutol hydrochloride in a
pharmaceutical formulation. Journal of Pharmaceutical and Biomedical Analysis,
2002; 27 (6): 995-1007.
Rajalahti T, Kvalheim OM. Multivariate data analysis in pharmaceutics: A tutorial
review. International Journal of Pharmaceutics, 2011; 417: 280-290.
Rang MJ, Miller CA. Spontaneous emulsification of oils containing hydrocarbon,
nonionic surfactant, and oleyl alcohol. Journal of Colloid and Interface Science,
1999; 209(1): 179-92.
Rao YM, Kumar MP, Apte S. Formulations of nanosuspensions of albendazole for
oral administration. Current Nanoscience, 2008; 4: 53-58.
Rasenack N, Hartenhauer H, Müller BW. Microcrystals for dissolution rate
enhancement of poorly water-soluble drugs. International Journal of Pharmaceutics,
2003; 254: 137-145.
Ravinchandra R. Studies on dissolution behaviour of nanoparticulate curcumin
formulation. Advances in Nanoparticles, 2013; 2: 51-59.
Reiss H. Entropy-induced dispersion of bulk liquids. Journal of Colloid and Interface
Science, 1975; 53(1): 61-70.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 267
Ringner M. What is principal component analysis? Nature Biotechnology, 2008; 26
(3): 303-304.
Rizwan M, Aqil M, Azeem A, Talegaonkar S, Sultana Y, Ali A. Enhanced
transdermal delivery of carvedilol using nanoemulsion as a vehicle. Journal of
Experimental Nanoscience, 2010; 5 (5): 390-411.
Roopwani R, Buckner IS. Understanding deformation mechanisms during powder
compaction using principal component analysis of compression data. International
Journal of Pharmaceutics, 2011; 418: 227-234.
Rowe RC, Sheskey PJ, Quinn ME (eds). Handbook of Pharmaceutical Excipients, 6th
ed. Pharmaceutical Press, Great Britain, 2009.
Saeedi M, Akbari J, Morteza-Semnani K, Enayati-Fard R, Sar-Reshteh-dar S,
Soleymani A. Enhancement of dissolution rate of indomethacin using liquisolid
compacts. Iranian Journal of Pharmaceutical Research, 2011; 10 (1): 25-34.
Sahoo NG, Kakran M, Shaal LA, Li L, Müller RH, Pal M, Tan LP. Preparation and
characterization of quercetin nanocrystals. Journal of Pharmaceutical Science, 2011;
100 (6): 2379-2390.
Salazar J, Ghanem A, Müller RH, Möschwitzer JP. Nanocrystals: comparison of the
size reduction effectiveness of a novel combinative method with conventional top-
down approaches. European Journal of Pharmaceutics and Biopharmaceutics, 2012;
81 (1): 82-90.
Salazar J, Heinzerling O, Müller RH, Möschwitzer JP. Process optimization of a
novel production method for nanosuspensions using design of experiments (DoE).
International Journal of Pharmaceutics, 2011; 420: 395-403.
Sander C, Holm P. Porous magnesium aluminometasilicate tablets as carrier of a
cyclosporine self-emulsifying formulation. AAPS PharmSciTech, 2009; 10 (4): 1388-
1395.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 268
Sanka K, Bandari S, Jukanti R, Veerareddy PR. Colon-Specific Microparticles of
Piroxicam: Formulation and Optimization Using 32 Factorial Design. Journal of
Dispersion Science and Technology, 2011; 32(10): 1396-1403.
Sanka K, Poienti S, Bari A, Diwan PV. Improved oral delivery of clonazepam
through liquisolid powder compact formulations: In-vitro and ex-vivo
characterization. Powder Technology, 2014; 256: 336-344.
Sayyad FJ, Tulsankar SL, Kolap UB. Design and development of liquisolid compact
of candesartan cilexetil to enhance dissolution. Journal of Pharmacy Research, 2013;
7 (5): 381-388.
Seo YG, Kim DW, Yousaf AM, Park JH, Chang P, Baek HH, Lim S, Kim JO, Yong
CS, Choi H. Solid self-nanoemulsifying drug delivery system (SNEDDS) for
enhanced oral bioavailability of poorly water-soluble tacrolimus: physicochemical
characterisation and pharmacokinetics. Journal of Microencapsulation, 2015; 32 (5):
503-510.
Serajuddin ATM. Salt formation to improve drug solubility. Advanced Drug Delivery
Reviews, 2007; 59: 603-616.
Shafiq S, Shakeel F, Talegaonkar S, Ahmad FJ, Khar RK, Ali M. Development and
bioavilability assessment of ramipril nanoemulsion formulation. European Journal of
Pharmaceutics and Biopharmaceutics, 2007; 66: 227-243.
Shah JC, Chen JR, Chow D. Metastable Polymorph of Etoposide with Higher
Dissolution Rate. Drug Development and Industrial Pharmacy, 1999; 25 (1): 63-67.
Shah SR, Parikh RH, Chavda JR, Sheth NR. Glibenclamide Nanocrystals for
Bioavailability Enhancement: Formulation Design, Process Optimization, and
Pharmacodynamic Evaluation. Journal of Pharmaceutical Innovation, 2014; 9 (3):
227-237.
Shah TJ, Amin AF, Parikh JR, Parikh RH. Process optimization and characterization
of poloxamer solid dispersion of a poorly water-soluble drug. AAPS PharmSciTech,
2007; 8 (2): E1-E7.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 269
Shahiwala A. Formulation approaches in enhancement of patient compliance to oral
drug therapy. Expert Opinion on Drug Delivery, 2011; 8(11): 1521-1529.
Shakeel F, Haq N, El-Badry M, Alanazi FK, Alsarra IA. Ultra fine super self-
nanoemulsifying drug delivery system (SNEDDS) enhanced solubility and dissolution
of indomethacin. Journal of Molecular Liquids, 2013; 180: 89-94.
Shanmugam S, Baskaran R, Balakrishnan P, Thapa P, Yong CS, Yoo BK. Solid self-
nanoemulsifying drug delivery system (S-SNEDDS) containing phophatidylcholine
for enhanced bioavailability of highly lipophilic bioactive carotenoid lutein. European
Journal of Pharmaceutics and Biopharmaceutics, 2011; 79 (2): 250-257.
Sharma A, Shanker C, Tyagi LK, Singh M, Rao CV. Herbal medicine for market
potential in India: An overview. Academic Journal of Plant Sciences, 2008; 1(2): 26-
36.
Sharma DK, Joshi SB. Solubility enhancement strategies for poorly water soluble
drugs in solid dispersions: A review. Asian Journal of Pharmaceutical Sciences,
2007; 1 (1): 9-19.
Sharma P, Zujovic ZD, Bowmaker GA, Marshall AJ, Denny WA, Garg S. Evaluation
of a crystalline nanosuspension: polymorphism, process induced transformation and
in-vivo studies. International Journal of Pharmaceutics, 2011; 408 (1-2): 138-151.
Shrivastava A, Kapadia U. Design, optimization, preparation and evaluation of
dispersion granules of valsartan and formulation into tablets. Current Drug Delivery,
2009; 6: 28-37.
Sigfridsson K, Lundqvist A, Strimfors M. Co-administration of a nanosuspension of a
poorly soluble basic compound and a solution of a proton pump inhibitor--the
importance of gastrointestinal pH and solubility for the in-vivo exposure. Drug
Development and Industrial Pharmacy, 2011; 37 (9): 1036-1042.
Sigfridsson K, Nordmark A, Theilig S, Lindahl A. A formulation comparison between
micro- and nanosuspensions: the importance of particle size for absorption of a model
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 270
compound, following repeated oral administration to rats during early development.
Drug Development and Industrial Pharmacy, 2011a; 37 (2): 185-192.
Sikarwar MS, Sharma S, Jain AK, Parial SD. Preparation, characterization and
evaluation of marsupsin–phospholipid complex. AAPS PharmSciTech, 2008; 9: 129-
137.
Singare DS, Marella S, Gowthamrajan K, Kulkarni GT, Vooturi R, Rao PS.
Optimization of formulation and process variable of nanosuspension: An industrial
perspective. International Journal of Pharmaceutics, 2010; 402 (1-2): 213-220.
Singh AK, Chaurasiya A, Singh M, Upadhyay SC, Mukherjee R, Khar RK.
Exemestane loaded self-microemulsifying drug delivery system (SMEDDS)
development and optimization. AAPS PharmSciTech, 2008: 9 (2): 628-634.
Singh B, Dahiya M, Saharan V, Ahuja N. Optimizing drug delivery systems using
systematic ‘design of experiments’. Part II: retrospect and prospects. Critical Review
in Therapeutic Drug Carrier System, 2005a; 22 (3): 215-294.
Singh B, Kumar R, Ahuja N. Optimizing drug delivery systems using systematic
“design of experiments.” Part I: Fundamental aspects. Critical Review in Therapeutic
Drug Carrier System, 2005; 22 (1): 27-105.
Singh B, Khurana L, Bandyopadhyay S, Kapil R, Katare OO. Development of
optimized self-nano-emulsifying drug delivery systems (SNEDDS) of carvedilol with
enhanced bioavailability potential. Drug Delivery, 2011; 18 (8): 599-612.
Singh SK, Ranjan P, Verma PRP, Razdan B. Glibenclamide-loaded self-
nanoemulsifying drug delivery system: development and characterization. Drug
Development and Industrial Pharmacy, 2010; 36 (8): 933-945.
Singh SK, Srinivasan KK, Gowthamarajan K, Singare DS, Prakash D, Gaikwad NB.
Investigation of preparation parameters of nanosuspension by top-down media milling
to improve thedissolution of poorly water-soluble glyburide. European Journal of
Pharmaceutics and Biopharmaceutics, 2011a; 78 (3): 441-446.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 271
Sofowora A, Ogunbodede E, Onayade A. The role and place of medicinal plants in
the strategies for disease prevention. African Journal of Traditional, Complementary
and Alternative Medicines, 2013; 10(5): 210-229.
Solutol® HS-15, Product Information Sheet, Signet, India, 2014.
Sonnergaard JM. Quantification of the compactibility of pharmaceuticals powders.
European Journal of Pharmaceutics and Biopharmaceutics, 2006; 62: 270-277.
Spireas S, Bolton M, Sanford M. Liquisolid Systems and Methods of Preparing Same.
U.S. Patent, 1999: US 5968550 A.
Spireas S, Bolton SM. Liquisolid systems and methods of preparing same. Europe
Patent, 2010: EP Patent 0946154 B1.
Spireas S. Liquisolid Systems and Methods of Preparing Same. U.S. Patent, 2002: US
6423339 B1.
Strickley RG. Currently marketed oral lipid based dosage forms: drug products and
excipients. In: Haus DJ (eds), Oral lipid-based formulations, enhancing the
bioavailability of poorly water soluble drugs. Informal Healthcare, Inc., New York,
2007: 1.31.
Sugimoto S, Niwa T, Nakanish Y, Danjo K. Novel ultra-cryo milling and co-grinding
technique in liquid nitrogen to produce dissolution-enhanced nanoparticles for poorly
water-soluble drugs. Chemical and Pharmaceutical Bulletin, 2012; 60 (3): 325-333.
Sun B, Yeo Y. Nanocrystals for the parenteral delivery of poorly water-soluble drugs.
Current Opinion in Solid State & Materials Science, 2012; 16 (6): 295-301.
Sun C, Grant DJW. Effects of initial particle size on the tableting properties of l-
lysine monohydrochloride dehydrate powder. International Journal of
Pharmaceutics, 2001; 215: 221-228.
Sun W, Mao S, Shi Y, Li LC, Fang L. Nanonization of itraconazole by high pressure
homogenization: stabilizer optimization and effect of particle size on oral absorption.
Journal of Pharmaceutical Sciences, 2011; 100 (8): 3365-3373.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 272
Sun W, Ni R, Zhang X, Li LC, Mao S. Spray drying of a poorly water-soluble drug
nanosuspension for tablet preparation: formulation and process optimization with
bioavailability evaluation. Drug Development and Industrial Pharmacy, 2015; 41 (6):
927-933.
Syed IA, Pavani E. The liquisolid technique: Based drug delivery system.
International Journal of Pharmaceutical Sciences and Drug Research, 2012; 4 (2):
88-96.
Tao Y, Jiangling W, Huibi X, Xiangliang Y. A new solid self-microemulsifying
formulation prepared by spray-drying to improve the oral bioavailability of poorly
water soluble drugs. European Journal of Pharmaceutics and Biopharmaceutics,
2008; 70: 439-444.
Tarr BD, Yalkowsky SH. Enhanced intestinal absorption of cyclosporine in rats
through the reduction of emulsion droplet size. Pharmaceutical Research, 1989; 6:
40-43.
Tayel SA, Soliman II, Louis D. Improvement of dissolution properties of
Carbamazepine through application of the liquisolid tablet technique. European
Journal of Pharmaceutics and Biopharmaceutics, 2008; 69: 342-347.
Teeranachaideekul V, Junyaprasert VB, Souto EB, Müller RH. Development of
ascorbyl palmitate nanocrystals applying the nanosuspension technology.
International Journal of Pharmaceutics, 2008; 354 (1-2): 227-234.
Tiong N, Elkordy AA. Effects of liquisolid formulations on dissolution of naproxen.
European Journal of Pharmaceutics and Biopharmaceutics, 2009; 73: 373-384.
Transcutol P, Product Information Sheet, BASF, India, 2013.
Valizadeh H, Nokhodchi A, Qarakhani N, Zakeri-Milani P, Azarmi S, Hassanzadeh
D, Löbenberg R. Physicochemical characterization of solid dispersions of
indomethacin with PEG 6000, Myrj 52, lactose, sorbitol, dextrin, and Eudragit E100.
Drug Development and Industrial Pharmacy, 2004; 30(3): 303-317.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 273
Van Citters GW, Lin HC. The Ileal Brake: A Fifteen-year Progress Report. Current
Gastroenterology Reports, 1999; 1(5): 404-409.
Van Eerdenbrugh B, Vermant J, Martens JA, Froyen L, Van Humbeeck J, Augustijns
P, Van den Mooter G. A screening study of surface stabilization during the production
of drug nanocrystals. Journal of Pharmaceutical Sciences, 2009; 98 (6): 2091-2103.
Vasconcelos T, Sarmento B, Costa P. Solid dispersion as strategy to improve oral
bioavailability of poor water soluble drugs. Drug Discovery Today, 2007; 12: 1068-
1075.
Vaskula S, Vemula S, Bontha V, Garepally P. Liquisolid compacts: An approach to
enhance the dissolution rate of Nimesulide. Journal of Applied Pharmaceutical
Science, 2012; 2: 115-121.
Venkatesh G, Majid MI, Mansor SM, Nair NK, Croft SL, Navaratnam V. In-vitro
and in-vivo evaluation of self-microemulsifying drug delivery system of
buparvaquone. Drug Development and Industrial Pharmacy, 2010; 36 (6): 735-745.
Verma S, Kumar S, Gokhale R, Burgess DJ. Physical stability of nanosuspensions:
investigation of the role of stabilizers on Ostwald ripening. International Journal of
Pharmaceutics, 2011; 406(1-2): 145-152.
Villar AM, Naveros BC, Campmany AC, Trenchs MA, Rocabert CB, Bellowa LH.
Design and optimization of self-nanoemulsifying drug delivery systems (SNEDDS)
for enhanced dissolution of gemfibrozil. International Journal of Pharmaceutics,
2012; 431 (1-2): 161-175.
Wang L, Dong J, Chen J, Eastoe J, Li X. Design and optimization of a new self-
nanoemulsifying drug delivery system. Journal of Colloid and Interface Science,
2009; 330: 443-448.
Wang L, Hao Y, Liu N, Ma M, Yin Z, Zhang X. Enhance the dissolution rate and oral
bioavailability of pranlukast by preparing nanosuspensions with high-pressure
homogenizing method. Drug Development and Industrial Pharmacy, 2012; 38 (11):
1381-1389.
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 274
Wang P, Luo Q, Miao Y, Ying L, He H, Cai C, Tang X. Improved dissolution rate
and bioavailability of fenofibrate pellets prepared by wet-milled-drug layering. Drug
Development and Industrial Pharmacy, 2012a; 38 (11):1344-1353.
Wang Y, Liu Z, Zhang D, Gao X, Zhang X, Duan C, Jia L, Feng F, Huang Y, Shen
Y, Zhang Q. Development and in-vitro evaluation of deacety mycoepoxydiene
nanosuspension. Colloids and Surfaces B, Biointerfaces, 2011; 83 (2): 189-197.
Wei Y, Ye X, Shang X, Peng X, Bao Q, Liu M, Guo M, Li F. Enhanced oral
bioavailability of silybin by a supersaturatable self-emulsifying drug delivery system
(S-SEDDS). Colloids and Surfaces A: Physicochemical and.Engineering Aspects,
2012; 396: 22-28.
Wu L, Zhang J, Watanabe W. Physical and chemical stability of drug nanoparticles.
Advanced Drug Delivery Reviews, 2011; 63: 456-469.
Xi J, Chang Q, Chan CK, Meng ZY, Wang GN, Sun JB, Wang YT, Tong HH, Zheng
Y. Formulation development and bioavailability evaluation of a self-nanoemulsified
drug delivery system of oleanolic acid. AAPS PharmSciTech, 2009; 10 (1): 172-182.
Xia D, Quan P, Piao H, Piao H, Sun S, Yin Y, Cui F. Preparation of stable
nitrendipine nanosuspensions using the precipitation-ultrasonication method for
enhancement of dissolution and oral bioavailability. European Journal of
Pharmaceutical Sciences, 2010; 40 (4): 325-334.
Xuemei W, Jianhua X, Xiuwang H, Caixia W. Self-microemulsifying drug delivery
system improves curcumin dissolution and bioavailability. Drug Development and
Industrial Pharmacy, 2011; 37 (1): 15-23.
Yeom DW, Song YS, Kim SR, Lee SG, Kang MH, Lee S, Choi YW. Development
and optimization of a self-microemulsifying drug delivery system for atorvastatin
calcium by using D-optimal mixture design. International Journal of Nanomedicine,
2015; 10: 3865-3878.
Yoo JH, Shanmugam S, Thapa P, Lee ES, Balakrishnan P, Baskaran R, Yoon
SK, Choi HG, Yong CS, Yoo BK, Han K. Novel self-nanoemulsifying drug delivery
Chapter 7 Bibliography
Komal Parmar, PhD Thesis
|Saurashtra University| 275
system for enhanced solubility and dissolution of lutein. Archives of Pharmacal
Research, 2010; 33 (3): 417-26.
Yosra SRE, Magda AE, Ossama YA. Self-nanoemulsifying drug delivery systems of
tamoxifen citrate: Design and Optimization. International Journal of Pharmaceutics,
2009; 380: 133–141.
Zhang D, Tan T, Gao L, Zhao W, Wang P. Preparation of azithromycin
nanosuspensions by high pressure homogenization and its physicochemical
characteristics studies. Drug Development Industrial Pharmacy, 2007; 33(5): 569-
575.
Zhang L, Chai G, Zeng X, He H, Xu H, Tang X. Preparation of fenofibrate immediate
release tablets involving wet grinding for improved bioavailability. Drug
Development and Industrial Pharmacy, 2010; 36 (9): 1054-1063.
Zhang N, She D, Hu L, Liu H. Preparation and Evaluation of Daidzein Loaded Self-
Microemulsifying Drug Delivery System. Applied Mechanics and Materials, 2012;
140 (2): 200-205.
Zhang P, Liu Y, Feng N, Xu J. Preparation and evaluation of self-microemulsifying
drug delivery system of oridonin. International Journal of Pharmaceutics, 2008; 355
(1-2): 269-276.
Zhao Y, Wang C, Chow AHL, Ren K, Gong T, Zhang Z, Zheng Y. Self-
nanoemulsifying drug delivery system (SNEDDS) for oral delivery of Zedoary
essential oil: Formulation and bioavailability studies. International Journal of
Pharmaceutics, 2010; 383: 170–177.
Zhu M, Ghodsi A. Automatic dimensionality selection from the scree plot via the use
of profile likelihood. Computational Statistics & Data Analysis, 2006; 51: 918- 930.
Zhu S, Hong M, Liu C, Pei Y. Application of Box-Behnken design in understanding
the quality of genistein self-nanoemulsified drug delivery systems and optimizing its
formulation. Pharmaceutical Development and Technology, 2009; 14 (6): 642-649.
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