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CHAPTER8
CHAPTER8
BIBILOGRAPHY
134 | P a g e
Department of pharmaceutics
8. Aulton ME. Pharmaceutics – The science of dosage form design. 2nd ed.
ed. New Dehi: Wolters Kluwer Pvt Ltd; 2008.p. 231- 232.
http://www.fda.gov/AboutFDA/CentersOffices/OfficeofMedicalProductsand
Tobacco/CDER/ucm128219.htm 88
14. Duncan QM Craig. The mechanism of drug release from solid dispersions in
144.
2007 5 9; 631-644.
of four poorly water soluble drugs by cogrinding with commonly used excipients.
136 | P a g e
Department of pharmaceutics
17. Gole and Lawrence, lyophilized technique for the fast dissolving solid dosage
18. Leon Lachman, Herbert A Lieberman, Joseph L Kanig. The Theory and
21. Amidon GL, Lennernas H, Shah VP, and Crison JR. Theoretical basis for a
rates of pharmaceuticals. Am J Pharm Sci Support Public Health 1963; 135: 78–
92.
23. Goldberg AH, Gibaldi M, Kanig JL. Increasing dissolution rates and
1965;54(8):1145-1148..
137 | P a g e
Department of pharmaceutics
25. Mayersohn M and Gibaldi M, new method of solid state dispersion for
27. Aulton ME. Pharmaceutics: The science of dosage form design. Churchill
308(1-2): 69-83.
bioavailability of poor water soluble drugs. Drug Discovery Today 2007; 12(23-
24): 1068-1075.
32. Mooter GP, Weuts I, Ridder T D and Blaton N. Evaluation of Inutec SP1 as a
new carrier in the formulation of solid dispersions for poorly soluble drugs. Intl J
138 | P a g e
Department of pharmaceutics
35. Johari GP, Kim S and Shanker RM. Dielectric studies of molecular motions in
94(10): 2207-2223.
technology, 2nd ed. New York: Marcel Dekker Inc., Basel; 2002. Vol. 1: p. 642-
646.
39. Leuner C and Dressman J. Improving drug solubility for oral delivery using
139 | P a g e
Department of pharmaceutics
114.
W-103, 2007.
140 | P a g e
Department of pharmaceutics
48. Goldberg AH, Gibaldi M, and Kanig JL. Increasing dissolution rates and
gastrointestinal absorption of drugs via solid solutions and eutectic mixtures. II.
49. Sameer H Lakade and Bhalekar M R. Different types of method for modified
dosage form for enhancement of dissolution rate through solid dispersion. IJPSR
51. Breitenbach J. Melt extrusion from process to drug delivery technology. Eur J
52. Narang A and Shrivastava A. Melt extrusion solid dispersion technique. Drug
53. Serajuddin A. Solid dispersion technique. J Pharm Sci 1999 ; 88(10) : 891-
900.
141 | P a g e
Department of pharmaceutics
Carbamazepine and PEG 4000 as a potential rapid release dosage form. Eur J
58. Deitzel JM, Kleinmeyer J, Harris D and Beck Tan NC. The effect of
supercritical fluid technology. Crit Rev Therpeutic Drug Carrier Syst. 2001;18(2):
173-199.
solid dispersion and lyophilization techniques. Int J Pharm 1995; 126: 155-160
142 | P a g e
Department of pharmaceutics
30: 530-531.
64. Lin CW and Cham TM. Effect of particle size on the available surface area of
399.
232.
197-204.
143 | P a g e
Department of pharmaceutics
solid dispersions of poorly water-soluble drugs with enteric coating agents. Chem
poorly soluble drug using solid dispersion technique. Chem Pharm Bull 1996; 44:
568-571.
72. Okonogi S et al. Improved dissolution of ofloxacin via solid dispersion. Int J
73. Mura P et al. Thermal behavior and dissolution properties of naproxen from
binary and ternary solid dispersions. Drug Dev Ind Pharm 1999; 25: 257-264.
74. Serajuddin Abu TM. Solid dispersion of poorly water-soluble drugs: Early
75. Seeger, H. "Drug delivery Products and the Zydis Fast-dissolving Dosage
375-382.
144 | P a g e
Department of pharmaceutics
tablets formulation, Drug Deed. India, Pharmacy -1997. issue 23, pp. 665-669.
research. 2 (4): 223–35.
research. 2 (4): 223–35.
2008-09-10. Retrieved 2009-01-10.
145 | P a g e
Department of pharmaceutics
2014-02-02. Retrieved 2009-01-09.
2009-09-20. Retrieved 2009-01-09.
2009-01-06. Retrieved 2009-01-10.
2008-05-09. Retrieved 2009-01-09.
2015-02-18. Retrieved 2009-01-09.
Livingstone; 1999:A51-A53.
146 | P a g e
Department of pharmaceutics
98.Wen H, Zhang HW, Muhmut M, Zou PF, New RRC, Craig PS. Initial
doi:10.1080/00034983.19 94.11812834
setid=e8941166-b77d-45aa-a6e8-04f1c0afd845.
when taken with a fatty meal. Eur J Clin Pharmacol. 1988. doi:10.1007/
BF00540964
147 | P a g e
Department of pharmaceutics
doi:10.1016/S0001- 706X(03)00031-7
water soluble drugs by cogrinding with commonly used excipients. Eur J Pharm
water soluble drugs by cogrinding with commonly used excipients. Eur J Pharm
106. Rowe et al., eds. Handbook of Pharmaceutical Excipients, 5th edn. London:
107.WIKIPEDIA
108. Rowe et al., eds. Handbook of Pharmaceutical Excipients, 5th edn. London:
109.WIKIPEDIA
110. Rowe et al., eds. Handbook of Pharmaceutical Excipients, 5th edn. London:
111.WIKIPEDIA
148 | P a g e
Department of pharmaceutics
112. Rowe et al., eds. Handbook of Pharmaceutical Excipients, 7th edn. London:
113.WIKIPEDIA
Sciences(2018);21(1):10-15.
Research(2016);5(8):1170-1181.
149 | P a g e
Department of pharmaceutics
(1), 2016,1-8.
2014;2(10):61-78.
state characterization and in-vitro dissolution study)., Int J Pharm Bio Sci 2013
2011, 2 (5):30-42 .
150 | P a g e
Department of pharmaceutics
378 .
albendazole solid dispersion with crystalline carriers., Indian J. Pharm. Sci., 2006,
68 (5): 599-607 .
130. Dan Liua., Increasing solubility and dissolution rate of drugs via eutectic
151 | P a g e
Department of pharmaceutics
(5): 129-132.
1(2):1-6.
152 | P a g e
Department of pharmaceutics
dispersion;IJSP:2011:10(11):13-14
153 | P a g e
Department of pharmaceutics
154 | P a g e