Author(s): Ashok Mahajan, Ashish Yadav, Priyal Patel, Shailesh Koradia, Falgun Mehta, Kautuk Shah

Email(s): apmcashok@gmail.com

DOI: 10.52711/0974-360X.2021.00335   

Address: Ashok Mahajan*, Ashish Yadav, Priyal Patel, Shailesh Koradia, Falgun Mehta, Kautuk Shah
Department of Pharmaceutics, Babaria Institute of Pharmacy, BITS Edu Campus, Vadodara- Mumbai NH-8, Varnama, Vadodara-391240, Gujarat, India.
*Corresponding Author

Published In:   Volume - 14,      Issue - 4,     Year - 2021


ABSTRACT:
The objective of present investigation was comparison of porous carriers to increase the dissolution properties of BCS class II drug Ziprasidone. Solvent evaporation method was used for the adsorption of ziprasidone on various porous carriers. Three different porous carriers namely Florite, Neusilin US2, Sylysia 350 were used in the study. Prepared microparticles were characterised for invitro drug release, SEM, XRD and DSC. The optimized formulation containing ziprasidone: florite microparticles had high drug release (94.88% in 45 min) than plain ziprasidone tablets (21.13% in 45 min) which is due to increase in surface area and decrease in crystallinity of drug after adsorption onto porous carrier.


Cite this article:
Ashok Mahajan, Ashish Yadav, Priyal Patel, Shailesh Koradia, Falgun Mehta, Kautuk Shah. Comparative Evaluation of Porous Carriers for Dissolution Improvement of BCS Class II Drug. Research Journal of Pharmacy and Technology. 2021; 14(4):1899-4. doi: 10.52711/0974-360X.2021.00335

Cite(Electronic):
Ashok Mahajan, Ashish Yadav, Priyal Patel, Shailesh Koradia, Falgun Mehta, Kautuk Shah. Comparative Evaluation of Porous Carriers for Dissolution Improvement of BCS Class II Drug. Research Journal of Pharmacy and Technology. 2021; 14(4):1899-4. doi: 10.52711/0974-360X.2021.00335   Available on: https://www.rjptonline.org/AbstractView.aspx?PID=2021-14-4-11


REFERENCES:
1. Ben JB et al. Successful oral delivery of poorly water-soluble drugs both depends on the intraluminal behavior of drugs and of appropriate advanced drug delivery systems. Eur J Pharm Sci. 2019; 137(1): 104967
2. Shinkar DM et al. Liquisolid Technology: A Review. Asian J. Res. Pharm. Sci. 2016; 6(3): 161-166
3. Nirmala D et al. Preparation and characterization of Pitavastatin solid dispersions. Preparation and characterization of Pitavastatin solid dispersions. Research Journal of Pharmacy and Technology. 2016; 9(8): 1023-1026
4. Nayak S et al. Nanosuspension – Preparation, In Vitro and Ex Vivo Evaluations of Felodipine Hydrochloride. Research Journal of Pharmacy and Technology. 2015; 8(1): 38-43
5. Patel S and Shah DP. A Review on Nanocrystals Drug Delivery System. Research Journal of Pharmacy and Technology. 2015; 8(5): 647
6. Deshmukh A et al. Formulation Development and In-vitro Evaluation of Self Micro-emulsifying Drug Delivery system (SMEDDS) of Antiretroviral. Research Journal of Pharmacy and Technology. 2012; 5(10): 1347-1351.
7. Earle RR et al. Enhancement of Dissolution Rate and Physicochemical Characterization of Irbesartan Inclusion. Complexes using Cyclodextrins. Research J. Pharm. and Tech. 2017; 10(1): 301-306.
8. Venkatesh et al. Preparation and Evaluation of Nateglinide-Cyclodextrin Inclusion Complex. Research Journal of Pharmacy and Technology. 2018; 11(3): 1017-1022.
9. Mahajan A et al. Solid dispersion adsorbate technique for improved dissolution and flow properties of lurasidone hydrochloride: characterization using 32 factorial design, Drug Development and Industrial Pharmacy, 2018; 44(3): 463-471
10. Shinkar DM et al. Solubility and dissolution enhancement of sulfasalazine by solid dispersion technique. Research Journal of Pharmacy and Technology. 2018; 11(4): 1227-1282.
11. Gao L. et al. Drug nanocrystals: in vivo performances. J. Control. Release 2012; 160: 418-430 
12. Patel HM et al. Nanosuspension Technologies for Delivery of Poorly Soluble Drugs- A Review. Research J. Pharm. and Tech. 2016; 9(5): 625-632.
13. Gabriel OKL et al. Enhancement of norfloxacin solubility via inclusion complexation with β cyclodextrin and its derivative hydroxypropyl-β-cyclodextrin, Asian Journal of Pharmaceutical Sciences. 2016; 11(4): 536-546.
14. Patil AL and Patil SS. Interaction of Lornoxicam with Natural Cyclodextrin in Solid and Solution State. Research Journal of Pharmacy and Technology. 2011; 4(10):1521-1525
15. Caputo G et al. Nimesulide adsorbed on silica aerogel using supercritical carbon dioxide. Chem. engineering Res. And design. 2012; 1082–1089
16. Ahuja G and Pathak K. Porous Carriers for Controlled/Modulated Drug Delivery. Indian J. Pharm. Sci. 2009; 71(6): 599-607.
17. Sharma S. et al. Adsorption of Meloxicam on porous Calcium Silicate characterization and tablet formulation. American APS Pharm. SciTech. 2005; 6(4): E618-E625.
18. Miaomiao Z. et al. Design and pharmaceutical applications of porous particles RSC Adv. 2017; 7:39490-39501
19. Paola M. et al. Characterization and evaluation of different mesoporous silica kinds as carriers for the development of effective oral dosage forms of glibenclamide. International Journal of Pharmaceutics. 2019; 563: 43-52
20. Jagtap RS et al. Adsorption of Nifedipine on Porous Calcium silicate for Enhancement of Solubility and Dissolution Rate. Research J. Pharm. and Tech. 2017; 10(1): 301-306.
21. Gauniya A. et al. Formulation, Optimization Characterization of Ziprasidone nanocrystals prepared by Media Milling Technique. Int. J. Pharmacy and Pharm Sci. 2015; 7(8): 146-150.
22. Emine T. Optimization and in vitro evaluation of ziprasidone nanosuspensions produced by a top-down approach. Journal of Drug Delivery Science and Technology. 2019; 52: 37-45
23. Miao Y. et al. Characterization and Evaluation of self-nanoemulsifying sustained-release pellet formulation of ziprasidone with enhanced bioavailability and no food effect. Drug Deliv. 2015; 1-10.
24. Karanth G. et al. Solid Oral Dosage Forms of Ziprasidone Containing Colloidal Silicone Dioxide. United States patent US20080268034 A1, 2008
25. Edit B. et al. Study of equilibrium solubility measurement by saturation shake-flask method using hydrochlorothiazide as model compound. Journal of Pharmaceutical and Biomedical Analysis. 2008; 46(2): 335-341.
26. Cuiyan H. et al. A Comparative Study of the Use of Mesoporous Carbon and Mesoporous Silica as Drug Carriers for Oral Delivery of the Water-Insoluble Drug Carvedilol. Molecules. 2019; 24: 1770.
27. United States Pharmacopeia-40, NF-35, United States Pharmacopeial Convention, Inc.; 2017.

Recomonded Articles:

Research Journal of Pharmacy and Technology (RJPT) is an international, peer-reviewed, multidisciplinary journal.... Read more >>>

RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

1.3
2021CiteScore
 
56th percentile
Powered by  Scopus


SCImago Journal & Country Rank

Journal Policies & Information


Recent Articles




Tags


Not Available