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Author(s): Shaikh Sadiya Mehmood1, Sayyed Simran S.2, Pathan Najiya S.3, Dr Aejaz Ahemed4

Email(s): 1sksadiya0986@gmail.com

Address:

    J.I.I.U' S Ali Allana College of Pharmacy Akkalkuwa, Dist. Nandurbar (425415), Maharashtra, India

Published In:   Volume - 2,      Issue - 5,     Year - 2023

DOI: Not Available

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ABSTRACT:
The various traditional and novel techniques that that can be used for solubility enhancement of BCS Class II drugs are briefly discussed in this article. Based on their solubility and permeability, drugs are typically divided into four classes (Classes I–IV) according to the biopharmaceutics Classification system (BCS). Of these classes, BCS class II drugs have high permeability and low solubility; not only do these characteristics constitute The rate-limiting step in the formulation of these drugs but the low solubility in water results in low bioavailability. Thus, methods for improving their solubility have been developed using lipid carriers such as niosomes, The Traditional techniques that has been use of co-solvents, Hydrotropy, Micronization, amorphous forms, use of surfactants, inclusion complex , use of soluble prodrugs, functional polymer technology, controlled precipitation technology. Niosomes technique is use to increase the bioavailability of Baloxavir and Efavirenz.

Cite this article:
Shaikh Sadiya Mehmood, Sayyed Simran S. , Pathan Najiya S. , Dr Aejaz Ahemed. A Review on Improve The Bioavailability of BCSS Class II Drug Baloxavir and Efavirenz. IJRPAS, Sep-Oct 2023; 2(5): 162-174 .


1.    Amidon GL, Lennernas H, Shah VP, Crison JR. A theoretical for a biopharmaceutics drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 1995;12:413-20.

2.    Chi-Yuan W, Benet LZ. Predicting drug disposition via application of BCS: Transport/Absorption/Elimination interplay and development of a biopharmaceutics drug disposition classification system. Pharm Res 2005;22:11-23.

3.    Kerns EH, Di L. Multivariate pharmaceutical profiling for drug discovery. Curr Top Med Chem 2002;2:87-98.

4.    Mujoriya RZ, Dhamande K, Bodla RB. Niosomal drug delivery system—a review. Int J Appl Pharm 2011;3:7-10.

5.    Rogerson A, Cummings J, Willmott N, Florence AT. The distribution of doxorubicin in mice following administration in niosomes. J Pharm Pharmacol 1988;40:337-42.

6.    Baillie AJ, Coombs GH, Dolan TF. Non-ionic surfactant vesicles, niosomes, as delivery system for the anti-leishmanial drug, sodium stibogluconate. J Pharm Pharmacol 1986;38:502-

7.    Khandare JN, Madhavi G, Tamhankar BM. Niosomes novel drug delivery system. Eastern Pharm 1994;37:61-4.

8.    Raja Naresh RA, Chandrashekhar G, Pillai GK, Udupa N. Anti inflammatory activity of niosome encapsulated diclofenac sodium with tween-85 in arthritic rats. Ind J Pharmacol 1994;26:46-8.

9.    Chauhan S, Luorence MJ. The preparation of polyoxyethylene containing non-ionic surfactant vesicles. J Pharm Pharmacol 1989;41:6p.

10.    Blazek Walsh AI, Rhodes DG. SEM imaging predicts the quality of niosomes from maltodextrin-based proniosomes. Pharm Res 2001;18:65661.

11.    Amidon GL, Lennernas H, Shah VP, Crison JR. A theoretical basis for a biopharmaceutics drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharm Res 1995;12:413–20.

12.    Guidance for industry, “Waiver of in vivo bioavailability and bioequivalence studies for immediate release solid oral dosage forms based on a biopharmaceutics classification system,” CDER/FDA; 2000.

13.    Biopharmaceutics classification system guidance office of pharmaceutical science, CDER/FDA; 2006. Obrenovic MM, Perrie Y, Gregoriadis G. Entrapment of plasmid DNA into niosomes: characterization studies. J Pharm Pharmacol 1998;50:155.

14.    . Brewer J, Alexander J. The adjuvant activity of non-ionic surfactant vesicles (niosomes) on the BALB/c humoral response to bovine serum albumin. Immunology 1992;75:570-5. Hassan Y, Brewer J, Alexander J, Jennings R. Immune responses in mice induced by HSV-1 glycoproteins presented with ISCOMs or NISV delivery systems. Vaccine 1996;14:1581-9.

15.    . Mohamedi S, Brewer J, Alexander J, Heath A, Jennings R. Antibody responses, cytokine levels and protection of mice immunized with HSV-2 antigens formulated into NISV or ISCOM delivery systems. Vaccine 2000;18:2083-94.

16.    Yoshioka T, Skalko N, Gursel M, Gregoriadis G, Florence A. A nonionic surfactant vesicle in-water-in-oil (v/w/o) system: potential uses in drug and vaccine delivery. J Drug Target 1995;2:533-9.

17.    17 .Murdan S, Gregoriadis G, Florence A. Sorbitan monostearate/polysorbate 20 organogels containing niosomes: a delivery vehicle for antigens. Eur J Pharm Sci 1999;8:177-86. Chambers MA, Wright DC, Brisker J, Williams A, Hatch G, Gavier

18.    Widen D, et al. A single dose of killed mycobacterium bovis BCG in a novel class of adjuvant (Novasome™) protects guinea pigs from lethal tuberculosis. Vaccine 2004;22:1063-71.

19.     Vangala A, Kirby D, Rosenkrands I, Agger EM, Andersen P, Perrie Y. A comparative study of cationic liposome and niosome-based adjuvant systems for protein subunit vaccines: characterization, environmental scanning electron microscopy and immunization studies in mice. J Pharm Pharmacol 2006:58:787-99.

20.    Vangala A, Bramwell VW, McNeil S, Christensen D, Agger EM, Perrie Y. Comparison of vesicle based antigen delivery systems for delivery of hepatitis B surface antigen. J Controlled Release 2007;119:102-10.

21.     Ferro V, Stimson W. Investigation into suitable carrier molecules for use in an antigonadotrophin releasing hormone vaccine. Vaccine 1998;16:1095-102.

22.     Ferro VA, Costa R, Carter KC, Harvey MJ, Waterston MM, Mullen AB, et al. Immune responses to a GnRH-based anti-fertility immunogen, induced by different adjuvants and subsequent effect on vaccine efficacy. Vaccine 2004;22:1024-31.

23.    Lezama Dávila CM. Vaccination of C57BL/10 mice against cutaneous leishmaniasis. Use of purified gp63 encapsulated into niosomes surfactants vesicles: a novel approach. Mem Inst Oswaldo Cruz 1999;94:67-70.

24.    Rentel C, Bouwstra J, Naisbett B, Junginger H. Niosomes as anovel peroral vaccine delivery system. Int J Pharm1999;186:161-7.

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