CRYSTAL FORMS OF LOMEFLOXACIN: PREPARATION, CHARACTERIZATION AND DISSOLUTION PROFILE

The present work was undertaken with the synthesis of crystal forms of Lomefloxacin from solvents of varying polarity (polar, protic solvents). The purpose of the present investigation was to employ crystallization techniques in order to improve the solubility and dissolution studies of Lomefloxacin...

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Main Authors: Vellaichamy Ganesan, Raju Thenge, Naresh Vinjamuri, Srinivasarao Prathipati
Format: Article
Language:English
Published: Universitas Gadjah Mada 2018-09-01
Series:Indonesian Journal of Pharmacy
Subjects:
Online Access:https://indonesianjpharm.farmasi.ugm.ac.id/index.php/3/article/view/615/490
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author Vellaichamy Ganesan
Raju Thenge
Naresh Vinjamuri
Srinivasarao Prathipati
author_facet Vellaichamy Ganesan
Raju Thenge
Naresh Vinjamuri
Srinivasarao Prathipati
author_sort Vellaichamy Ganesan
collection DOAJ
description The present work was undertaken with the synthesis of crystal forms of Lomefloxacin from solvents of varying polarity (polar, protic solvents). The purpose of the present investigation was to employ crystallization techniques in order to improve the solubility and dissolution studies of Lomefloxacin. The experimental methods involved the preparation of lomefloxacin crystals by crystallization from single solvent technique. Crystals were prepared from solvents like distilled water, ethanol and methanol. Prepared crystals were undergone various studies in terms of crystal yield, melting point, true density, solubility and in vitro drug release study as well as characterized by technique viz: FT-IR, differential scanning calorimetry (DSC) and Powder X-ray Diffractometry(PXRD). Photomicrographs of the crystals shows that the crystals obtained from different solvents existed in different shape. Among all the crystals, LOME-I belongs to Type-1 and LOME–II belongs to Type-2 based on instrumental techniques. Highest crystal yield (88%) and maximum density (1.2021g/mL) was observed with LOME-I. Maximum solubility and dissolution rate was observed in LOME-III followed by LOME-II and LOME-I. However all prepared crystal forms showed higher solubility and dissolution profile when compare with commercial Lomefloxacin. It is concluded that the study has indicated the existence of two polymorphic forms of Lomefloxacin which was having better solubility and in vitro release than that of commercial Lomefloxacin.
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spelling doaj.art-4b3dec55e6ad4d49bc1052cdfc515e522022-12-21T17:33:10ZengUniversitas Gadjah MadaIndonesian Journal of Pharmacy2338-94272338-94862018-09-01244238244http://dx.doi.org/10.14499/indonesianjpharm0iss0pp238-244CRYSTAL FORMS OF LOMEFLOXACIN: PREPARATION, CHARACTERIZATION AND DISSOLUTION PROFILEVellaichamy Ganesan0Raju Thenge1Naresh Vinjamuri2Srinivasarao Prathipati3Department of Pharmaceutics, The Erode College of Pharmacy and Research Institute, Erode, Tamil Nadu, India – 638112Department of Pharmaceutics, The Erode College of Pharmacy and Research Institute, Erode, Tamil Nadu, India – 638112Department of Pharmaceutics, The Erode College of Pharmacy and Research Institute, Erode, Tamil Nadu, India – 638112Department of Pharmaceutics, The Erode College of Pharmacy and Research Institute, Erode, Tamil Nadu, India – 638112The present work was undertaken with the synthesis of crystal forms of Lomefloxacin from solvents of varying polarity (polar, protic solvents). The purpose of the present investigation was to employ crystallization techniques in order to improve the solubility and dissolution studies of Lomefloxacin. The experimental methods involved the preparation of lomefloxacin crystals by crystallization from single solvent technique. Crystals were prepared from solvents like distilled water, ethanol and methanol. Prepared crystals were undergone various studies in terms of crystal yield, melting point, true density, solubility and in vitro drug release study as well as characterized by technique viz: FT-IR, differential scanning calorimetry (DSC) and Powder X-ray Diffractometry(PXRD). Photomicrographs of the crystals shows that the crystals obtained from different solvents existed in different shape. Among all the crystals, LOME-I belongs to Type-1 and LOME–II belongs to Type-2 based on instrumental techniques. Highest crystal yield (88%) and maximum density (1.2021g/mL) was observed with LOME-I. Maximum solubility and dissolution rate was observed in LOME-III followed by LOME-II and LOME-I. However all prepared crystal forms showed higher solubility and dissolution profile when compare with commercial Lomefloxacin. It is concluded that the study has indicated the existence of two polymorphic forms of Lomefloxacin which was having better solubility and in vitro release than that of commercial Lomefloxacin.https://indonesianjpharm.farmasi.ugm.ac.id/index.php/3/article/view/615/490PolymorphismSolubilityDissolution rateDSCFT-IRPXRD
spellingShingle Vellaichamy Ganesan
Raju Thenge
Naresh Vinjamuri
Srinivasarao Prathipati
CRYSTAL FORMS OF LOMEFLOXACIN: PREPARATION, CHARACTERIZATION AND DISSOLUTION PROFILE
Indonesian Journal of Pharmacy
Polymorphism
Solubility
Dissolution rate
DSC
FT-IR
PXRD
title CRYSTAL FORMS OF LOMEFLOXACIN: PREPARATION, CHARACTERIZATION AND DISSOLUTION PROFILE
title_full CRYSTAL FORMS OF LOMEFLOXACIN: PREPARATION, CHARACTERIZATION AND DISSOLUTION PROFILE
title_fullStr CRYSTAL FORMS OF LOMEFLOXACIN: PREPARATION, CHARACTERIZATION AND DISSOLUTION PROFILE
title_full_unstemmed CRYSTAL FORMS OF LOMEFLOXACIN: PREPARATION, CHARACTERIZATION AND DISSOLUTION PROFILE
title_short CRYSTAL FORMS OF LOMEFLOXACIN: PREPARATION, CHARACTERIZATION AND DISSOLUTION PROFILE
title_sort crystal forms of lomefloxacin preparation characterization and dissolution profile
topic Polymorphism
Solubility
Dissolution rate
DSC
FT-IR
PXRD
url https://indonesianjpharm.farmasi.ugm.ac.id/index.php/3/article/view/615/490
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AT rajuthenge crystalformsoflomefloxacinpreparationcharacterizationanddissolutionprofile
AT nareshvinjamuri crystalformsoflomefloxacinpreparationcharacterizationanddissolutionprofile
AT srinivasaraoprathipati crystalformsoflomefloxacinpreparationcharacterizationanddissolutionprofile