Floating microspheres of lafutidine: formulation, optimization, characterization, in-vitro and in-vivo floatability studies using eudragit grades (Record no. 17323)

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control field 20220825133841.0
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fixed length control field 220825b 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 Floating microspheres of lafutidine: formulation, optimization, characterization, in-vitro and in-vivo floatability studies using eudragit grades
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(3), Jul-Sep
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 681-688p.
520 ## - SUMMARY, ETC.
Summary, etc. Aim/Background: The objective behind this study was to develop a Microspheres of
Lafuditine using central composite design for gastroretentive drug delivery. Materials and
Methods: Gastroretentive Microspheres were prepared by Emulsion Solvent Evaporation
method. The present investigation will study the effect of formulation variables (polymer
concentration etc) on the floating behaviour and drug release characteristics for developing
mathematical relationship between them and optimize the formulation with an aim to
minimize onset of floatation, maximize the duration of floatation in stomach in order to
achieve maximum bioavailability and therapeutic efficacy of selected drug. Microspheres
were evaluated for shape, size, melting point, buoyancy time, floating capacity, % yield,
swelling index, and
in-vitro drug release and in-vivo kinetic studies. Results: Results
showed that selected independent variables significantly affect the yield (66-85%),
particle size (3.78-10.62 μm), buoyancy (42.68-95.75%), encapsulation efficiency
(69.32–94.05%), and cumulative drug release from the microspheres (79.02-96.92%).
The interface and quadratic terms were also affect the process variables, it can be said
that to develop and optimize gastroretentive system of Lafuditine with central composite
design (CCD) is a valuable second-degree design which is effective treatment of
H. pylori
mediated infection and also provides a base to localize the drug release in the gastric
region. Conclusion: The gastroretentive floating Microparticulate system of Lafutidine will
enhance the patient compliance and play a vital role in improving patient’s quality of life.
Keywords: Lafutidine, Eudragit, Central composite design,
In-vitro drug release,
Microparticulate system, Sodium bicarbonate.
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) 4645
Co-Author Tiwari, Abhishek
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-56-3-681.pdf
Link text Click here
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Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2022-08-25 2022-1373 2022-08-25 2022-08-25 Articles Abstract Database
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