Development of ph sensitive polymeric nanoparticle of erythromycin (Record no. 16973)

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control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220629160213.0
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fixed length control field 220629b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 16913
Author Thaarani, B.
245 ## - TITLE STATEMENT
Title Development of ph sensitive polymeric nanoparticle of erythromycin
250 ## - EDITION STATEMENT
Volume, Issue number Vol.15(4), Oct-Dec
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. M P
Name of publisher, distributor, etc. BRNSS Publication Hub.
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 413-419p.
520 ## - SUMMARY, ETC.
Summary, etc. Introduction: Erythromycin is a macrolide antibiotic used for the treatment of various infections caused by
bacteria. It is also used for Respiratory tract infection, skin infection, syphilis, etc. Erythromycin base was a
poorly water-soluble and acid-labile drug. The bioavailability of Erythromycin was very less about (15–35%). The
absorption site of Erythromycin is the small intestine. pH-responsive polymeric drug delivery system is efficient
delivering the acid instable drugs. Aim: The main objective of the study is to formulate Erythromycin loaded
pH-responsive polymeric nanoparticles was prepared using pHresponsive polymer to prevent the degradation
of acid-labile drug and to evaluate the Polymeric nanoparticle. Materials and Methods: The Erythromycin
Polymeric nanoparticles were prepared by Nano precipitation method using Eudragit L100 as a Polymer and
polyvinyl alcohol (PVA) as stabilizer. The particle size, polydispersity index (PDI), zeta potential, entrapment
efficiency and In-vitro drug release studies were performed for nanoparticle. The compatibility between drug and
polymer was studied by Fourier transform infrared. The nanoparticle was lyophilized and surface morphology
was determined by scanning electron microscope. Excipients were added and formulated into tablet. The
Precompression evaluation of lyophilized powder was carried out. The post-compression evaluation for tablets
and In-vitro release study was performed and compared with marketed tablet. Results: Erythromycin nanoparticle
was formulated and evaluated. It showed the particle size of 270.2 nm with PDI of 0.166 and the zeta potential was
found to be −32.5. The Entrapment efficiency of the ENP 9 Nanoparticle was 96%. Erythromycin loaded tablet
was formulated and evaluated for hardness, weight variation, disintegration, friability, thickness, and diameter. It
was present within the limit. In vitro drug release of the formulated tablet showed 91% drug release in phosphate
buffer pH6.8 at the end of 60 min. Conclusion: Erythromycin nanoparticles were in the nanometer range and it
was stable. Polymeric nanoparticle tablet had the ability to protect the acid-labile drug and it gets dissolved in
the intestine pH 6.8. The nano particulate tablet showed the better release when compared with marketed tablet.
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) 16904
Co-Author Subramanian, S.
773 0# - HOST ITEM ENTRY
Title International journal of green pharmacy
Place, publisher, and date of publication Mandsaur B.R. Nahata Smriti Sansthan
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.greenpharmacy.info/index.php/ijgp/article/view/3193
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
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 2022-06-29 2022-0970 2022-06-29 2022-06-29 Articles Abstract Database
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