REFERENCES:
1. Peppas N. A., and Langer R., New challenges in biomaterials, Science, 1994, 263; 1715-1720.
2. Zhidong L., jaiwei L., Shufang N., Hui L., Pingtian D., Weisan P., Study of an alginate/HPMC based in situ gelling ophthalmic delivery system for gatifloxacin, Int. J. Pharm., 2006, 315; 12-17.
3. Sarasija S., and Shyamala B., Nasal Drug Delivery: An overview, Indian J. Pharm. Sci., 2005, 67; 19-25.
4. Wataru K., Yashiro K., Miyazaki S., Attwood D., In situ gelling pectin formulations for oral sustained delivery of paracetamol, Drug Develop. Ind. Pharm., 2004, 30; 593-602.
5. Rathod H., Patel V., Modasia M., In situ gel as a novel approach of gastroretentive drug delivery, International Journal of Pharmacy and Life Sciences, 2010, 1(8); 440-447.
6. Esposito E. and Carratto V., Comparative analysis of tetracycline containing dental gels; poloxomers and mono-glycerides based formulation, Int. J. Pharm., 1996, 142; 9-23.
7. Geraghaty P. and Attwood D., An investigation of parameters influencing the bioadhesive properties of myverol 18-99/ water gels. Biomaterials, 1997, 18; 63-70.
8. Motto F.and Gailloud P., In-vitro assessment of new embolic liquids prepared from preformed polymers and water miscible solvents aneurysm treatment, Biomaterials, 2000, 21; 803-811.
9. Bhardwaj T. R., kanwar M., Lal R., Gupta A., Natural gums and modified natural gums as sustained release carriers, Drug Devel. Ind. Pharm., 2000, 26; 1025-1038.
10. Guo J., Skiner G., Harcum W., BAmum P., Pharmaceutical applications of naturally occurring water soluble polymers. Pharm. Sci. & Technol. Today, 1998, 1; 254-261.
11. Podual K., and Peppas N. A., Dynamic behavior of glucose oxidase-containing microparticles of poly(ethylene.-grafted cationic hydrogels in an environment of changing pH, Biomaterials, 2000, 21; 1439-1450.
12. Burkoth A., and Anseth K., A review of photocrosslinked polyanhydrides: In situ forming degradable networks, Biomaterials, 2000,21, 23952404.
13. Sawhney A. and Pathak C., Photopolymerizable biodegradable hydrigels as tissue containing materials and controlled release carriers, US Patent 5410016, 1995.
14. Taylor L. and Cerankowski L., preparation of films exhibiting a balanced temperature dependence to permeation by aqueous solutions – a study of lower consolute behavior, J. Polym. Sci. Polym. Chem. Ed., 1975, 13; 2551-2570.
15. Heskins M. and Guillet J., Solution properties of poly(N-isopropylacrylamide., J. Macromol. Sci. Chem., 1968, 2; 1441-1455.
16. Qiu Y. and Park K., Environment-sensitive hydrogels for drug delivery, Adv. Drug Deliv. Rev., 2001, 53; 321-339.
17. Soppimath K., Aminabhavi T., Dave A., Kumbar S., Rudzinski W., Stimulus-responsive – smart hydrogels as novel drug delivery systems, Drug Dev. Ind. Pharm., 2002, 28; 957-974.
18. Aikawa K., Mitsutake A., Uda H., Tanaka S., Shimamura H., Aramaki Y., Drug release from pH-response polyvinylacetal diethyl aminoacetate hydrogel, and application to nasal delivery, Int. J. Pharm., 1998, 168; 181-189.
19. Alexandridis P. and Lindman B., Amphiphilic block polymers, Amsterdam:Elsvier.
20. Dumitriu S., Vidal P. F., Chornet E., Hydrogels based on polysaccharides in medical applications, New York, Marcel Dekker Inc., 1996; 125-242.
21. Ni Y., Kenneth M. Y., In-situ gel formation of pectin 2004, United States Patent 6777000.
22. Wataru K., Yasuhiro K., Miyazaki S., Attwood D., In situ gelling pectin formulations for sustained delivery of paracetamol. Drug Develop. Ind. Pharm., 2004, 30; 593-599.
23. Miyazaki S., Suisha F., Kawasaki N., Thermally reversible xyloglucan gels as vehicles for rectal delivery, J. Control Rel., 1998, 56; 75-83.
24. Kawasaki N., Ohkura R., Miyazaki S., Uno Y., Sugomoto S., Attwood D., Thermal reversible xyloglucan gels as vehicles for oral drug delivery, Int. J. Pharm., 1999, 181; 227-234.
25. Suisha F., Kawasaki N., Miyazaki S., Shirakawa M., Yamotoya K., Sasaki M., Xyloglucan gels as sustained release vehicles for intraperitoneal administration of mitomycin C, Int. J. Pharm., 1998, 172; 27-32.
26. Miyazaki S., Suzuki S., Kawasaki N., Endo K., Takahashi A., Attwood D., In situ gelling xyloglucan formulations for sustained release ocular delivery off pilocarpine hydrochloride, Int. J. Pharm., 2001, 229; 29-36.
27. Itoh K. and Yahaba M., In situ gelling xyloglucan/pectin formulations for oral sustained drug delivery, Int. J. Pharm., 2008, 356; 95-101.
28. Miyazaki S., Hirotatsu A., Kawasaki N., Attwood D., In situ gelling gellan formulations as vehicles for oral drug delivery, J. Control Rel., 1999, 60, 287-295.
29. Crescenzi V., Dentini M., Coviello T., Solutions and gelling properties of microbial polysaccharides of industrial interest: The case of gellan. In: Dawes EA, editor, Novel biodegradable microbial polymers, Dordrecht: Kluwer Academic Publishers, 199; 227-284.
30. Sechoy O., Tissie G., Sebastian C., Maurin F., Driot J. Y., Trinquand C., A new long acting ophthalmic formulation of carteolol containing Alginic acid. Int. J. Pharm., 2000, 207; 109-116.
31. Nakamura K., Nishimura Y., Hatakeyama H., Hatakeyama T., Thermal properties of water insoluble alginate films containing di- and tri-valent cations, Thermochim. Acta, 1995, 267; 343-353.
32. Bhardwaj L., Sharma P.K., Malviya R., A short review on gastro retentive formulations for stomach specific drug delivery: special emphasis on floating in situ gel system, African journal of basic and applied sciences, 2011, 3(6); 300-312.
33. Wong W., Chan L., Kho S., Heng P.W., Design of controlled-release solid dosage forms of alginate and chitosan using microwave, J. Contolled Release, 2002, 84; 99-114.
34. Al-Shamklani A., Bhakoo M., Tuboku M. A., Duncan R., Evaluation of the biological properties of alginates and gellan and xanthum gum, Proc. Int. Symp. Control Release Bioact. Material, 1991, 18; 213-214.
35. Modasiya M. K., Prajapati B.G., Patel V. M., Patel J. K., Sodium alginate based in situ gelling system of famotidine: preparation and in-vivo characterizations, e-Journal of Science and Technology, 2010, 5(1); 27-42.
36. Kashyap N., Viswanad B., Sharma G., Bhardwaj V., Ramarao P., Kumaar M. N., design and evaluation of biodegradable, biosensitive in situ gelling systems for pulsatile delivery of insulin, Biomaterials, 2007, 28; 2051-2060.
37. Khan A. D., Bajpai M., Floating drug delivery system: an overview, International journal pharmtech and research, 2010, 2(4); 2497-2505.
38. google.com/patents/US6777000.
39. google.com/patents/US7971848.
40. Rey-Rico A., Silva Maite, Couceiro J., Concheiro A., Alvarenz-Lorenzo C., Ostreogenic efficacy of in situ gelling poloxamine systems with and without bone morphogenetic protein – 2, European Cells and Materials,2011, 21; 317-340.
41. Rehman T. U., Tavelin S., Grobner G., Chitosan in situ gelation for improved drug loading and retention in poloxamer 407 gels, International journal of pharmaceutics, 2011, 409; 19-29.
42. Kazarian S. G., Velasco D., Danoux C. B., Redondo J. A., Elvira C., Rom J. S., Wray P. S., pH-sensitive polymer hydrogels derived from morpholine to prevent the crystallization of ibuprofen, Journal of Controlled Release, 2011, 149; 140-145.
43. Pate D. M., Patel D. K., Patel C. N., Formulation and evaluation of floating oral in situ gelling system of amoxicillin, 2011, 276250, 8 pages, doi:10.5402/2011/276250.
44. Shah S., Upadhayay P., Parikh D., Shah J., In situ gel: A novel approach of gastroretentive drug delivery, Asian journal of biomedical and pharmaceutical sciences, 2012, 2(8.; 1-8.
45. Bhardwaj L., Sharma P. K., Malviya R., A short review on gastro retentive formulations for stomach specific drug delivery: Special emphasis on floating in situ gel system, African journal of basic and applied sciences, 2011, 3(6); 300-312.