Formulation and Characterization of Chitosan Microparticulate System Using Central Composite Design for the Drug: Lafutidine (Record no. 15552)

MARC details
000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20211123100139.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 211123b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 11968
Author Sunil Kumar
245 ## - TITLE STATEMENT
Title Formulation and Characterization of Chitosan Microparticulate System Using Central Composite Design for the Drug: Lafutidine
250 ## - EDITION STATEMENT
Volume, Issue number Vol.55(2), Apr-Jun
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Banaglore
Name of publisher, distributor, etc. Association of Pharmaceutical Teachers of India (APTI)
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 354-362p.
520 ## - SUMMARY, ETC.
Summary, etc. Aim: To formulate a Micro particulate system using central composite design to remain in the stomach for prolonged time and used for Gastroretentive drug delivery. Materials and Methods: Gastroretentive Microspheres were prepared by Emulsion Solvent Evaporation. Micro particulate system were evaluated for micro meritic study, percentage yield, drug entrapment efficiency, in-vitro buoyancy, surface morphology, in-vitro drug release, in-vivo floating study and stability studies. Results: The micro meritic parameters of floating microspheres were found to be within the acceptable limits. The particle size of microspheres was found to be in the range 3.43–15.38 μm. The entrapment efficiency was found to be in the range of 72.02–95.02%. The floating microspheres were spherical in shape with distinct pores, slightly rough surface when observed under scanning electron microscopy. The percentage yield was found to be in the range of 68–89%. The in-vitro buoyancy was found to be in the range of 55.67–92.55% and a total buoyancy time of more than 10 h. The in-vitro dissolution studies showed a cumulative % release in the range of 77.67–95.41%. The optimized formulation F4 was floating in rat stomach for almost 8 h. All the formulations followed Korsemeyer- Peppas kinetics indicating drug release by non-fickian release mechanism. The stability studies showed that floating microspheres were stable at 40 ± 2°C. Conclusion: The optimized formulation showed good floating for 12 h in stomach of rat. The formulation was able to treat the alcohol induced ulcer and also found good stability.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 14747
Co-Author Goyal, Naveen
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
International Standard Serial Number 0019-5464
Title Indian journal of pharmaceutical education and research
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-55-2-354.pdf
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 23/11/2021   2021-2022357 23/11/2021 23/11/2021 Articles Abstract Database
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