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References
|
Al-Hamidi H, Edwards A, Mohammad A, Nokhodchi A (2010). To enhance dissolution rate of poorly water-soluble drugs: Glucosamine hydrochloride as a potential carrier in solid dispersion formulations. Colloids and Surfaces B: Biointerfaces 76(1):170-178. |
|
|
Bhardwaj P, Singh R, Swarup A (2012). International Journal of Pharmaceutical Sciences and Research 3(3):934. |
|
|
Bharti P, Attal RV, Munde VA, Birajdar SA, Bais S (2015). Strategies to Enhance Solubility and Dissolution of a poorly water soluble drug. Journal of Innovations in Pharmaceuticals and Biological Sciences 2(4):482-494. |
|
|
Chan S, Chung Y, Cheah X, Tan E, Quah J (2015). The characterization and dissolution performances of spray dried solid dispersion of ketoprofen in hydrophilic carriers. Asian journal of Pharmaceutical Sciences 10:372-385. |
|
|
Choi J, Park J (2017). Design of PVP/VA S-630 based tadalafil solid dispersion to enhance the dissolution rate. European Journal of Pharmaceutical Sciences 9:269-276. |
|
|
FDA (2017). Waiver of in Vivo Bioavailability and Bioequivalence Studies for Immediate Release Solid Oral Dosage Forms based on a Biopharmaceutics Classification System Guidance for Industry. |
|
|
Frizon F, Josimar E, Oliveira D, Carmen M, Marcia L, Juliana M (2013). Dissolution rate enhancement of loratadine in polyvinylpyrrolidone K-30 solid dispersions by solvent methods. Powder Technology 235:532-539. |
|
|
Ganesan P, Soundararajan R, Shanmugam U, Vinothini R (2015). Development, characterization and solubility enhancement of comparative dissolution study of second generation of solid dispersions and microspheres for poorly water soluble drug. Asian Journal of Pharmaceutical Sciences 10(5):433-441. |
|
|
Gaur PK, Mishra S, Bajpai M (2014). Formulation and evaluation of controlled release of telmisartan microsphere: In vitro/in vivo study. Journal of Food and Drug Analysis 22(4):542-548. |
|
|
Kala S, Juyal D (2016). Preformulation and characterization studies of aceclofenac active ingredient. The Pharma Innovation Journal 5(9):110-119. |
|
|
Kannan K, Karar PK, Manvalan R (2009). Formulation and evaluation of sustained-release microspheres of acetazolamide by solvent evaporation technique. Journal of Pharmaceutical Sciences and Research 1(1):36. |
|
|
Kawabata Y, Wada K, Nakatani M, Yamada S, Onoue S (2011). Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications. International Journal of Pharmaceutics 420:1-10. |
|
|
Kurmi R, Mishra D.K, Jain D.K (2016). Solid Dispersion: A Novel Means of Solubility Enhancement. Journal of Critical Reviews 3(1):1-8. |
|
|
Leonardi D, Barrera M.G, Lamas M.C, and Salomon C.J (2007). Development of prednisone: Polyethylene glycol 6000 fast-release tablets from solid dispersions: Solid-state characterization, dissolution behavior, and formulation parameters. American Association of Pharmaceutical Scientists 8(4):221. |
|
|
Leuner C, Dressman J (2000). Improving drug solubility for oral delivery using solid dispersions. European Journal of Pharmaceutics and Biopharmaceutics 50:47-60. |
|
|
Madgulkar A, Bandivadekar M, Shid T, Rao S (2016). Sugars as solid dispersion carrier to improve solubility and dissolution of the BCS class II drug: clotrimazole. Drug development and Industrial Pharmacy 42(1):28-38. |
|
|
Milling EL (1991). Microencapsulation In.: Lachman L, Lieberman HA, editors. The theory and practice of industrial pharmacy. 2nd ed. Mumbai, India: Varghese Publishing House:26-7. |
|
|
Mogal S, Gurjar P, Yamgar D, Kamod A (2012). Solid dispersion technique for improving solubility of some poorly soluble drugs. Scholars Research Library. Der Pharmacia Letter 4(5):1574-1586. |
|
|
Mooter GV (2011). The use of amorphous solid dispersions: a formulation strategy to overcome poor solubility and dissolution rate. Drug Discovery Today: Technologies 9(2):79-85. |
|
|
Pande SV, Biyani KR (2014). Solid Dispersion: An Effective Approach for Bioavailability Enhancement for Poorly Soluble Drugs. American Journal of Pharmacy and Health research 2(7). |
|
|
Patel A, Ray S, Thakur RS (2006). In-vitro evaluation and optimization of controlled release floating drug delivery system of metformin hydrochloride. DARU 14(2):57-64. |
|
|
Rane Y, Mashru R, Sankalia M, Sankalia J (2007). Effect of Hydrophilic swellable polymers on dissolution enhancement of carbamazepine solid dispersions studied using response surface methodology. Aaps Pharmscitech 8(2):E1-E11 |
|
|
Samal HB, Debata J, Kumar N, Sneha S, Patra PK (2012). Solubility and dissolution improvement of Aceclofenac using cyclodextrin. International Journal of Drug Delivery and Research 4(4):326-333. |
|
|
Singh BM, Kim KH (2000). Floating drug delivery systems: an approach to oral controlled drug delivery via gastric retention Journal of Controlled Release 63(3):235-259. |
|
|
Srivastava AK, Ridhurkar DN, Wadhwa S (2005). Floating microspheres of cimetidine: formulation, characterization and in vitro evaluation. Acta Pharmaceutica 55(3):277-285. |
|
|
Weerapol Y, Limmatvapirat S, Nunthanid J, Konthang S, Suttiruengwang S, Sriamornsak P (2017). Development and characterization of nifedipine-amino methacrylate copolymer solid dispersion with various adsorbents. Asian Journal of Pharmaceutical Sciences 12:343-335. |
|
|
Yadav P, Kumar V, Singh P, Bhatt HR, Mazumder B (2013). Physicochemical characterization and in vitro dissolution studies of solid dispersions of ketoprofen with PVP K30 and D-mannitol. Saudi Pharmaceutical Journal 21:77-84. |
|
|
Zaini F, Umar S, Firdaus N (2017). Improvement of dissolution rate of valsartan by solid dispersion system using D-mannitol. Asian Journal of Pharmaceutical and Clinical Research 10:3. |
|
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