Reference

1. Hite, M. Federici, and S. Turner, 2003. Delivery of poorly soluble medications orally in part 1. Issue 1–3. Pharmaceutical production and packaging sourcer.
2. Hu, J., K.P. Johnston, and R.O. Williams III, 2004. Int. J. Pharm. 271, 145–154, Fast dissolving high strength danazol granules generated by spray freezing into liquid technique.
3. Low water solubility- an industry-wide challenge in drug administration, Am. Pharm. Rev. 5, 82-85, 2002. Lipinski, C.
4. Solid dispersions: A Review, Pak. J. Pharm. Sci. 22 (2), 234–246. Dhirendra, K., Lewis, S., Udupa, N., and Atin, K.
5. Bioavailability and bioequivalence testing by Malinowski, H.J. The Science and Practice of Pharmacy by Remington. 20th edition in Gennaro AR, editor 2000; 995–1004; Philadelphia: Lippincott Williams Wilkinson.
6. Increasing medication solubility for oral administration using solid dispersions. Leuner, C., Dressman, J. 2000. 50, 47–60 Eur. J. Pharm. Biopharm.
7. Amidon, G.L., H. Lenneranas, V. P. Shah, and J. R. Crison, 1995. The relationship between in vivo bioavailability and in vitro drug product dissolution serves as the theoretical foundation for a biopharmaceutical drug categorization. 12(3), 413–420 J. Pharm. Res.
8. Lyophilization of polyethylene glycol mixtures, Dannenfelser, R.M., Zielinski, J., and Wang, B. (2004). J. Pharm. Sci. 93, 2244–2249.
9. Roseman, T.J., and S.H. Yalkowsky, 1981. Cosolvents are used to cosolve medicines. Methods of Soluhilization of Medicines, S.H. Yalkowsky, ed. New York, Dekker.
10. Singh, B., Ahuja, N., and Katare, O.P., 2007. studies on the use of water-soluble carriers to improve medication solubility and mathematical modelling of drug release. 65, 26–38 Eur. J. Pharm. Biopharm.
11. J.C. Chaumeil, 1998. Techniques and Results in Experimental and Clinical Pharmacology. 20, 211-215. Micronisation: a way of enhancing the bioavailability of poorly soluble medicines.
12. Mallikarjun, V., Areefulla, S.H., and Babu, V.R. 2010. Overview of Solubility and Dissolution Improvement. J Pharm Res 3 (1): 141–145.
13. V. Bakatselou, R. C. Oppenheim, and J. B. Dressman, 1991. Bile salts' solubilization and wetting effects on the breakdown of steroids. Drug Research, 8, 1461-1469.
14. Challa, R. Ahuja, J. Ali, and R. K. Khar, 2005. Revised Review on Cyclodextrins in Drug Delivery. 6(2), 29-57. AAPS PharmSciTech. 14) Challa, R. Ahuja, J. Ali, and R. K. Khar, 2005. Revised Review on Cyclodextrins in Drug Delivery. 6(2), 29-57. AAPS PharmSciTech.
15. Talari, R., Varshosaz, J., Mostafavi, S.A., Nokhodchi, A., 2009. Gliclazide Dissolution Enhancement Utilizing pH Adjustment Method in the Presence of Twelve Stabilizers with Different Physico-Chemical Properties. J Pharm Pharmaceut Sci. 12(3), 250 - 265.
16. Lachman, L., H.A. Lieberman, and J.L. Kanig, 1990. Industrial pharmacy: Theory and Practice. Varghese Publishing Company, Bombay, 3rd edition, 177.
17. Hussain, A., and Rytting, J.H., "Prodrug Approach to Enhancing Rate of Allopurinol Dissolution," 1974. 63(5), 798–799, J Pharm Sci.
18. J.M. Vaughn, X. Gao, M.J. Yacaman, K.P. Johnston, and R.O. Williams, 2005. Using cutting-edge Z-contrast STEM and complementary methods, powder generated by evaporative precipitation into aqueous solution (EPAS) and spray freezing into liquid (SFL) technologies are compared. 81–89 in Eur J Pharm Biopharm 60(1).
19. Spireas, S., C. I. Jarowski, and D. I. Rohera, 1992. Technology for powdered solutions: concepts and workings. Drug Research 9, 1351–1368.
20. Y. Javadzadeh, M. R. Siahi-Shadbad, M. Barzegar-Jalali, and A. Nokhodchi, 2005. improved piroxicam dissolving rate using liquisolid compacts. 60, 361-365 Farmaco.
21. In 2005, Nokhodchi, A., Javadzadeh, Y., Siahi- Shadbad, M.R., and Barzegar-Jalali, M. The impact of vehicle type and concentration on the rate of indomethacin's dissolution from liquisolid compacts. 8,18–25 J Pharm Pharm Sci.
22. Rades, T., Hempenstall, J., Scott, A., Sertsou, G., 2002. Drug incorporation into solid solutions with HPMCP is influenced by a number of variables during solvent change coprecipitation. International Journal of Pharmaceutical Sciences, 245, 99–108.
23. 1994 Gabmann, P., List, M., Schweitzer, A., and Sucker. Options to parenteral administration of medications with limited water solubility include hydrosols. 40, 64–72, Eur. J. Pharm. Biopharm
24. High Pressure Process Technology: Foundations and Applications, A. Bertucco and G. Vetter, 2001. Elsevier, Amsterdam, Industrial Chemistry Library, 9, 1-3.
25. New drug delivery systems for insoluble pharmaceuticals, Chowdary, K.P.R., and Madhavi, B.L.R., 2005. Medicines in India, 42(9), 557-564.
26. Lipid formulations for oral drug administration: nonemulsifying, self-emulsifying, and "self-microemulsifying" drug delivery methods (Pouton, W.C., 2000). S93–S98 in Eur. J. Pharm. Sci.
27. Lipid based formulations for intestinal lymphatic distribution, Eur. J. Pharm. Sci. 15, 405–415 (O'Driscoll, C. M. 2002).
28. Lipids, lipophilic medicines, and oral drug delivery—some new concepts, Charman, W.N. 2000. J. Pharm. Sci. 89, 967-978.
29. In 2007, Trevaskis, N.L., Charman, W.N., and Porter, C.J.H. Optimizing the oral delivery of lipophilic medicines with lipids and lipid-based formulations, Nature Rev. Drug Disc. 6, 231-248.
30. Dangi, J.S., S.P. Vyas, and V.K. Dixit, 1998. mixed micelles' function in medication delivery. First, soluble. 24, 681-684, Drug Dev. Ind. Pharma.
31. Chiou, W.L., Riegelman, S., 1971. Pharmaceutical uses of solid dispersion systems. J. Pharmac. Sci. 60(9), 1281–1302.
32. Sekiguchi, K., and N. Obi, 1961. Research on Eutectic Mixture Absorption. I. A comparison of how eutectic mixtures of sulfathiazole and regular sulfathiazole affect a person. Chem. Pharm. Bull. 9, 866-872.
33. Melt extrusion: from process to drug delivery method. Eur J Pharm Biopharm. 54 (2), 107-117, 2000. Breitenbach, J.
34. The 1960 publication Some Pharmaceutical Properties of Novobiocin by Mullins, J.D., and Macek, T.J. 49, 245-248 J. Am. Pharm. Assoc. Sci. Ed.
35. The 1965 publication by Goldberg, A.H., Gibaldi, and Kanig. increasing medication gastric absorption and dissolution rates using solid solutions and eutectic mixes. I. Discussion of the literature and theoretical considerations. J. Pharmaceutical Science 54(8), 1145–1148.
36. Solid-liquid equilibria in solutions of non-electrolytes were first described by Rastogi, R.P., and Rama Varma, K.T. in 1956. 2, 2097–2101 in J. Chem. Soc.
37. Dissolution rates of high energy polyvinylpyrrolidone (PVP)-sulfathiazole coprecipitates, Simonelli, A.P., Mehta, SC, Higuchi, W.I., 1969. 58(5), 538-549, J. Pharm. Sci.
38. 1966 paper by Goldberg, A.H., Gibaldi, and Kanig. Urea-acetaminophen system experimental study of increasing dissolving rates and gastrointestinal absorption of medicines via solid solutions and eutectic mixes. 55, 482-487 J. Pharm. Sci.
39. Formulation and dissolving properties of several fast-release solid griseofulvin dispersions, Chiou, W.L., and Riegelman, 1969. 1505–1510 in J. Pharm. Sci