SIMULTANEOUS COCRYSTALLIZATION AND MICRONIZATION OF PARACETAMOL-DIPICOLINIC ACID BY SUPERCRITICAL ANTISOLVENT (SAS)

Paracetamol (PCA) is the widely used analgesic and antipyretic drug. In the market, PCA exist as polymorph form I which have poor tabletability. The aim of this study was to improve the tabletability of PCA by using cocrystallization method with dipicolinic acid (DPA) and to evaluate the influence o...

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Main Author: Hiendrawan, Stevanus
Format: Theses
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/78630
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:78630
spelling id-itb.:786302023-11-01T13:51:21ZSIMULTANEOUS COCRYSTALLIZATION AND MICRONIZATION OF PARACETAMOL-DIPICOLINIC ACID BY SUPERCRITICAL ANTISOLVENT (SAS) Hiendrawan, Stevanus Indonesia Theses paracetamol, dipicolinic acid, cocystaf, tabletability, dissolution rate INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/78630 Paracetamol (PCA) is the widely used analgesic and antipyretic drug. In the market, PCA exist as polymorph form I which have poor tabletability. The aim of this study was to improve the tabletability of PCA by using cocrystallization method with dipicolinic acid (DPA) and to evaluate the influence of cocrystal preparation process in the physicochemical propefties of PCA-DPA cocrystal. PCA-DPA cocwstal were prepared using two different process namely rapid solvent evaporation and supercritical antisolvent (SAS). The cocystals were further characterized by powder X-ray diffraction (PXRD), thermal analysis (DSC, and TGA), cold contact method, microscopy analysis (polarized microscopy, and SEM), fomier transform infrared spectroscopy (FTIR), particle size distributions analysis. Flowability, compressibility, dissolution rate, and solubility study of cocrystals were evaluated in com arison to PCA. Distinct PXRD patterns from starting components indicated the formation of new crystalline phase. PXRD analysis showed that products obtained from each method have identical spectra. DSC themograms of PCA-DPA-RE and PCADPA-SAS cocrystal showed a sharp melting endotherm at 193.57 oc dan 194.13 oc which were different from the starting components. FTIR analysis provided clues about the fonnation of amide-carboxylic acid heterosynthon between PCA and DPA. Cocrystal produced by SAS have smaller average particle size than those produced by rapid solvent evaporation process as shown from particle size analysis. Tabletability study revealed superior tableting performance of both cocrystals compare to PCA. PCA-DPA-SAS and PCA-DPA-RE cocrystal show significant enhancement in the dissolution rate approximately 2.45 and 1.72 times compare to PCA alone. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Paracetamol (PCA) is the widely used analgesic and antipyretic drug. In the market, PCA exist as polymorph form I which have poor tabletability. The aim of this study was to improve the tabletability of PCA by using cocrystallization method with dipicolinic acid (DPA) and to evaluate the influence of cocrystal preparation process in the physicochemical propefties of PCA-DPA cocrystal. PCA-DPA cocwstal were prepared using two different process namely rapid solvent evaporation and supercritical antisolvent (SAS). The cocystals were further characterized by powder X-ray diffraction (PXRD), thermal analysis (DSC, and TGA), cold contact method, microscopy analysis (polarized microscopy, and SEM), fomier transform infrared spectroscopy (FTIR), particle size distributions analysis. Flowability, compressibility, dissolution rate, and solubility study of cocrystals were evaluated in com arison to PCA. Distinct PXRD patterns from starting components indicated the formation of new crystalline phase. PXRD analysis showed that products obtained from each method have identical spectra. DSC themograms of PCA-DPA-RE and PCADPA-SAS cocrystal showed a sharp melting endotherm at 193.57 oc dan 194.13 oc which were different from the starting components. FTIR analysis provided clues about the fonnation of amide-carboxylic acid heterosynthon between PCA and DPA. Cocrystal produced by SAS have smaller average particle size than those produced by rapid solvent evaporation process as shown from particle size analysis. Tabletability study revealed superior tableting performance of both cocrystals compare to PCA. PCA-DPA-SAS and PCA-DPA-RE cocrystal show significant enhancement in the dissolution rate approximately 2.45 and 1.72 times compare to PCA alone.
format Theses
author Hiendrawan, Stevanus
spellingShingle Hiendrawan, Stevanus
SIMULTANEOUS COCRYSTALLIZATION AND MICRONIZATION OF PARACETAMOL-DIPICOLINIC ACID BY SUPERCRITICAL ANTISOLVENT (SAS)
author_facet Hiendrawan, Stevanus
author_sort Hiendrawan, Stevanus
title SIMULTANEOUS COCRYSTALLIZATION AND MICRONIZATION OF PARACETAMOL-DIPICOLINIC ACID BY SUPERCRITICAL ANTISOLVENT (SAS)
title_short SIMULTANEOUS COCRYSTALLIZATION AND MICRONIZATION OF PARACETAMOL-DIPICOLINIC ACID BY SUPERCRITICAL ANTISOLVENT (SAS)
title_full SIMULTANEOUS COCRYSTALLIZATION AND MICRONIZATION OF PARACETAMOL-DIPICOLINIC ACID BY SUPERCRITICAL ANTISOLVENT (SAS)
title_fullStr SIMULTANEOUS COCRYSTALLIZATION AND MICRONIZATION OF PARACETAMOL-DIPICOLINIC ACID BY SUPERCRITICAL ANTISOLVENT (SAS)
title_full_unstemmed SIMULTANEOUS COCRYSTALLIZATION AND MICRONIZATION OF PARACETAMOL-DIPICOLINIC ACID BY SUPERCRITICAL ANTISOLVENT (SAS)
title_sort simultaneous cocrystallization and micronization of paracetamol-dipicolinic acid by supercritical antisolvent (sas)
url https://digilib.itb.ac.id/gdl/view/78630
_version_ 1822995830584377344