1. Yasir M, Mohd A, Ashwani K, Abhinav A:
Biopharmaceutical Classification System: An
Account International Journal of PharmTech
Research. 2010; 1681-1690.
2. Mahesh Kumar K and Anil B:
Biopharmaceutics drug disposition
classification system: An Extension of
Biopharmaceutics classification system,
International research journal of pharmacy
ISSN ;2230-8407.
3. Vikash D and Asha K: Role of
Biopharmaceutical Classification System In
Drug Development Program journal of
current pharmaceutical research JCPR 2011;
5: 28-31
4. Anuj K, Sangram K, Kumud P, Prithi P,
Singh K, Ajit S and Naveen P:Review On
Solubility Enhancement Techniques For
Hydrophobic Drugs
.PharmacieGlobaleInternational Journal Of
Comprehensive Pharmacy 2011; 976-8157.
5. Prudhvi Raj V, Subhashis D, Maleswari T,
NiranjanBabu M, BhaskarNaik B.
6. Preparation, Characterization And
Evaluation Of Olmesartan Medoxomil-Β
Cyclodextrin Complexes, Indian Journal Of
Research In Pharmacy And Biotechnology
Issn: 2321-5674
7. Ketan T. Savjani, Anuradha K. Gajjar, and
Jignasa K. Drug Solubility: Importance and
Enhancement Techniques. International
Scholarly Research Network ISRN
Pharmaceutics Volume 2012, Article ID
195727.
8. Kumari R, Chandel P, Kapoor A:
Paramount Role of Solid Dispersion in
Enhancement of Solubility, Indo Global
Journal of Pharmaceutical Sciences 2013; 3:
78-89.
9. Kalia A, Poddar M: Solid Dispersions: An
approach towards enhancing dissolution
rate. Int J Pharm Pharm. Sci 2011; 3: 9-19.
10. Kalyanwat R, Patel S. Solid Dispersion: A
method for enhancing drug dissolution. Int.
J. Drug Form. Res 2010; 1: 1-14.
11. Kamalakkannan V, Puratchikody A,
Masilamani K, Senthilnathan B. Solubility
enhancement of poorly soluble drugs by
solid dispersion technique – A review. J
Pharm Res 2010; 3: 2314-2321
12. Amit C, Upendra N, Neha G, SharmaVK
and KhosaR L:Enhancement of solubilization
and bioavailability of poorly soluble drugs
by physical and chemical modifications: A
recent review Journal of Advanced
Pharmacy Education & Research 2012;2: (1)
32-67.
13. Mohanachandran PS, Sindhumol PG and
Kiran TS: Enhancement Of Solubility And
Dissolution Rate: An Overview
Research Article CODEN: IJPRNK ISSN: 2277-8713
Nalla Sriraviteja, IJPRBS, 2013; Volume 2(5):182-203 IJPRBS
Available Online at www.ijprbs.com
201
Mohanachandran P S Et Al. /
PharmacieGlobale (Ijcp) 2010; 4 (11)
14. Varun Raj V, Venkateshwarlu L and
Srikanth L: Solubility Enhancement
Techniques, International Journal Of
Pharmaceutical Sciences Review And
Research2010; 5: 1
15. http://www.pharmainfo.net/reviews/so
lubilization-poorly-soluble-drugs-review
16. Solubility.
http://www.sciencebyjones.com/Teaching
%20Menu.htm
17. Solubility of Solutes and Aqueous
Solutions.
http://www.chem.lsu.edu/lucid/tutorials/tu
torials.html
18. Adam M. Persky and Jeffrey A. Hughes,
Solutions and Solubility.
http://www.cop.ufl.edu/safezone/prokai/p
ha5100/pha5110.htm
19. Singha lD and Curatolo W: Drug
polymorphism and dosage form design: a
practical perspective. Adv Drug Deliv Rev
2004; 56: 335-347.
20. Pinnamaneni S, Das NG and Das SK:
Formulation approaches for orally
administered poorly soluble drugs.
Pharmazie 2002; 57: 291 – 300.
21. Chaumeil JC: Micronisation: a method of
improving the bioavailability of poorly
solubledrugs, Methods and Findings in
Experimental and Clinical Pharmacology
1998; 20: 211-215.
22. Nanosuspension drug delivery
Technology and application - Nanotech -
Express Pharma Pulse.htm,
http://www.expresspharmapulse.com
23. Aulton ME: Pharmaceutics The science
of dosage form design, 2nd edition,
Churchill Livingstone. London 2002; 113 –
138: 234 – 252.
24. Joseph T:Rubino,Cosolvents and
Cosolvency 2002; 1: 658-670.
http://www.dekker.com
25. Jeffrey W. Millard FA, Alvarez-Nuezand
Yalkowsky SH: Solubilization by cosolvents
Establishing useful constants for the log
/linear model, International Journal of
Pharmaceutics 2002; 245: 153-166.
26. Lynn LB and Michael FC: NanoBio
Convergence – Emerging Diagnostic and
Therapeutic Applications. bioprocessing &
biopartnering 2006; 1-4.
27. Valizadeh H, Nokhodchi A, Qarakhani N,
et al: Physicochemical characterization of
solid dispersions of indomethacin PEG
6000n Myrj 52 lactose sorbitol dextrin and
Eudragit E100. Drug DevInd Pharm 2004;
30: 303-317.
28. Keck CM and Müller RH: Drug
nanocrystals of poorly soluble drugs
produced by high pressure homogenisation.
Eur J Pharm Biopharm 2006; 62: 3-16.
Research Article CODEN: IJPRNK ISSN: 2277-8713
Nalla Sriraviteja, IJPRBS, 2013; Volume 2(5):182-203 IJPRBS
Available Online at www.ijprbs.com
202
29. Izhar Ahmed and PavaniE: The Liquisolid
Technique: Based Drug Delivery System,
International Journal of Pharmaceutical
Sciences and Drug Research 2012; 4(2): 88-
96
30. MudgalSSand Pancholi SS, Formulation
of glibenclamide solid dispersions by
solvent evaporation technique Journal of
Chemical and Pharmaceutical Research
2012; 4(1):353-359.
31. The science and practices of pharmacy
by Remington-21 edition volume –I, page
no: 229-230.
32. The theory and practice of industrial
pharmacy by Lachman, page no:466-467.
33. Indian pharmacopeia volume-I, page
no:158.
34. Pharmaceutical excipients-4th edition,
editorial by Raymond C Rower, Paul J
Sheskey and Paul J Weller. page no:508-
513,484-487,479-483.
35. The complete drug reference by
martindale-34thedition,page no:45.3-47
36. Pharmaceutical statistics practical and
clinical application by sam ford Boltan,
Charles Bon, page no:222-239.
37. Basic statistics and pharmaceutical
statistical application by 2nd edition by
James E De muth. Research journal of
pharmaceutical, biological and chemical
sciences. Jan-March 2012 vol-3page no:
190.
38. Chowdary KPR ,Surya PRK, A factorial
study on the effect of β-Cyclo dextran and
poly xamv on the solubility and dissolution
rate of piroxicam. IJRPC 2011 :601-605
39. Chowdary KPR., Udaya Chowdary D and
Indira M, A factorial study on formulation
dept. Of ibuprofen tablet employing
ibuprofen starch 1500 and PVP K 30.IJPSR
2012; 3:189-193.
40. KPR Chowdary :A factorial study on
enhancing the dissolution rate of
nimesulide tablet employing starch citrate-
A new modified starch, PEG 400 PVP K 30.
IJPR&D 2011; 3:224-230
41. Harisshoaib M, Jaweria T, Hamid AM
and Rabiaismail Y:Evalution of drug released
kinetics from ibuprofen matrix tablet using
HPMC sut 2006; 19(2):119-124.
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