Novel glibenclamide–phospholipid complex for diabetic treatment: formulation, physicochemical characterization, and in-vivo evaluation (Record no. 17325)

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040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 17593
Author Rathor, Sandeep
245 ## - TITLE STATEMENT
Title Novel glibenclamide–phospholipid complex for diabetic treatment: formulation, physicochemical characterization, and in-vivo evaluation
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 697-705p.
520 ## - SUMMARY, ETC.
Summary, etc. Introduction: Formulation of phospholipid complex is an ideal approach to improve the
solubility of poorly soluble drugs. Objectives: This study has been aimed to prepare a novel
glibenclamide-phospholipid complex by using the solvent evaporation technique. Materials
and Methods: Because glibenclamide is a weakly soluble medication, complexing it with
phospholipids is an excellent way to enhance its solubility. The phospholipid complex
of Glibenclamide was produced using the solvent-evaporation technique to enhance its
oral efficacy. The formulation was characterized and evaluated by various parameters
including FTIR, DSC, PXRD, SEM, TEM,
in vitro drug release, and
in vivo pharmacokinetic
studies in Wistar rats plasma. According to studies, the Glibenclamide phosphates
combination is significantly more water-soluble than the physical combination and pure
Glibenclamide. The oral bioavailability of the glibenclamide-phospholipids complex was
measured by using HPLC in Wistar rats’ plasma. Results: There was no substantial
interaction between the medication and the phospholipid in the formulation, according
to the FTIR and PXRD findings. The morphology of the formulation was verified by
SEM and TEM investigations, indicating that the crystalline form had been converted
to an amorphous form. The glibenclamide-phospholipids complex had a greater peak
plasma concentration (5.1 vs. 3.8 g/mL), its AUC was higher (14.65 vs. 11.81 μgh/L),
and its T1/2 was longer (2.4 vs. 3.1 hr), showing that it enhanced drug dissolution
rate. Conclusion: The findings showed that increasing the oral bioavailability of water-
insoluble medicines by phospholipid-complexation is a potential approach. The results
showed that phospholipid-complexation may be used to enhance the oral bioavailability
of water-insoluble drugs.
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) 17594
Co-Author Bhatt, D.C.
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
Title Indian journal of pharmaceutical education and research
International Standard Serial Number 0019-5464
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-3-697_0.pdf
Link text Click here
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          School of Pharmacy School of Pharmacy Archieval Section 2022-08-25 2022-1375 2022-08-25 2022-08-25 Articles Abstract Database
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