Development and evaluation of nanosuspension incorporated in situ gel of brimonidine tartarate for ocular drug delivery (Record no. 17602)

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fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220922141719.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220922b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 18039
Author Hanagandi, Viresh
245 ## - TITLE STATEMENT
Title Development and evaluation of nanosuspension incorporated in situ gel of brimonidine tartarate for ocular drug delivery
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(1), Jan-Mar
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Karnataka
Name of publisher, distributor, etc. Association of Pharmaceutical Teachers of India (APTI)
Year 2022
300 ## - PHYSICAL DESCRIPTION
Pagination 94-102p.
520 ## - SUMMARY, ETC.
Summary, etc. Objectives: The goal of the study was to develop, optimize and<br/>in vitro-<br/>ex vivo<br/>investigation of Brimonidine tartrate nanosuspension incorporated<br/>in situ gel formulation<br/>to differentiate with marketed (formulation) eye drops for the efficient treatment of<br/>glaucoma. Materials and Methods: Nanosuspensions were formulated by solvent<br/>evaporation method using probe sonication technique. The effect of the independent<br/>variables Tween 80 and Pluronic F68 concentration on Nanosuspension properties were<br/>investigated by performing 32 factorial design of experiment. Nanosuspensions were<br/>characterized by measuring particle diameter and zeta potential, surface morphology,<br/>drug entrapment efficiency and then nanosuspensions were incorporated in to<br/>in situ gel<br/>base for<br/>in vitro release and<br/>ex-vivo corneal permeability studies and were differentiated<br/>with marketed product. Results and Discussion: The most excellent nanosuspension<br/>formulation system selected via the Design Expert 12 software program was F7 which<br/>contains 0.5% of Tween 80 and 3 % of Pluronic F68. An optimized nanosuspension<br/>formulation F7 showed an average particle diameter of 157.4±0.95 nm with PDI of<br/>0.379 and a zeta potential of -19.1 mV. It had an average entrapment efficiency of<br/>85.95±1.40%. It also showed 98.36±0.58% of drug being released<br/>in vitro when<br/>incorporated in to<br/>in situ gel base over 24 hr. F7 showed significantly greater drug<br/>permeation in comparison to the marketed eye drop formulation in<br/>ex vivo transcorneal<br/>permeability studies and was able of retaining its stability for 90 days. Conclusion: The<br/>developed nanosuspension incorporated<br/>in situ gel base formulation could be utilized as<br/>potential delivery system for long time management of glaucoma with once daily dose.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4755
Topical term or geographic name entry element PHARMACOGNOSY
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 9980
Co-Author Patil, Archana Sidagouda
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-56-1-94.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 22/09/2022   2022-1704 22/09/2022 22/09/2022 Articles Abstract Database
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