FORMULATION AND EVALUATION OF NAPROXEN AND L-TRYPTOPHAN COCRYSTAL

The poor solubility and low oral bioavailability of active pharmaceutical ingredients (APIs) pose significant challenges in product development, particularly for drugs classified as Biopharmaceutic Classification System (BCS) Class II. Various strategies have been explored to improve the physicochem...

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Main Author: Yuliza Putri, Diana
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/82660
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Institution: Institut Teknologi Bandung
Language: Indonesia
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spelling id-itb.:826602024-07-09T14:09:17ZFORMULATION AND EVALUATION OF NAPROXEN AND L-TRYPTOPHAN COCRYSTAL Yuliza Putri, Diana Indonesia Final Project Naproxen, Cocrystal, Aqueous solubility, Dissolution rate, Physicochemical characteristic, Compactibility INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/82660 The poor solubility and low oral bioavailability of active pharmaceutical ingredients (APIs) pose significant challenges in product development, particularly for drugs classified as Biopharmaceutic Classification System (BCS) Class II. Various strategies have been explored to improve the physicochemical properties of APIs, one of which is cocrystal formation. Cocrystallization offers a promising approach to enhance the physicochemical properties of drug products, including bioavailability, compactibility, and stability, without altering the pharmacological profile of the API. Naproxen, a nonsteroidal anti-inflammatory drug (NSAID) belonging to BCS Class II, exhibits poor compactibility. This study aims to investigate the formation of naproxen (NPX) cocrystals with L-tryptophan (TRY) and to evaluate their physicochemical properties. NPX-TRY cocrystals were prepared using the slurry method with a 1:1 molar ratio in two different solvents: ethanol and water. Cocrystals were characterized using Powder X-Ray Diffraction (PXRD), Scanning Electron Microscope (SEM), Fourier Transform Infrared (FTIR), and Differential Scanning Calorimetry (DSC). The solubility, dissolution rate, and compactibility profiles of the cocrystals were evaluated and compared to pure naproxen. PXRD results of cocrystals demonstrated distinct diffraction patterns from its components. DSC thermogram revealed the melting point of NPX-TRY water slurry to be 204,96°C, while the NPX-TRY ethanol slurry exhibited a melting point of 201,99°C. Notably, the solubility of the NPX-TRY ethanol and water slurry increased by 9,52 and 3,06 times, respectively. The intrinsic dissolution test conducted in a pH 7,4 phosphate buffer medium demonstrated a dissolution rate of 0,77 mg cm-2min-1 for NPX-TRY water slurry and 0,59 mg cm-2 min-1 for NPX-TRY ethanol slurry after 45 minutes. However, the compactibility profiles of both cocrystals were improved compared to pure naproxen. 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 The poor solubility and low oral bioavailability of active pharmaceutical ingredients (APIs) pose significant challenges in product development, particularly for drugs classified as Biopharmaceutic Classification System (BCS) Class II. Various strategies have been explored to improve the physicochemical properties of APIs, one of which is cocrystal formation. Cocrystallization offers a promising approach to enhance the physicochemical properties of drug products, including bioavailability, compactibility, and stability, without altering the pharmacological profile of the API. Naproxen, a nonsteroidal anti-inflammatory drug (NSAID) belonging to BCS Class II, exhibits poor compactibility. This study aims to investigate the formation of naproxen (NPX) cocrystals with L-tryptophan (TRY) and to evaluate their physicochemical properties. NPX-TRY cocrystals were prepared using the slurry method with a 1:1 molar ratio in two different solvents: ethanol and water. Cocrystals were characterized using Powder X-Ray Diffraction (PXRD), Scanning Electron Microscope (SEM), Fourier Transform Infrared (FTIR), and Differential Scanning Calorimetry (DSC). The solubility, dissolution rate, and compactibility profiles of the cocrystals were evaluated and compared to pure naproxen. PXRD results of cocrystals demonstrated distinct diffraction patterns from its components. DSC thermogram revealed the melting point of NPX-TRY water slurry to be 204,96°C, while the NPX-TRY ethanol slurry exhibited a melting point of 201,99°C. Notably, the solubility of the NPX-TRY ethanol and water slurry increased by 9,52 and 3,06 times, respectively. The intrinsic dissolution test conducted in a pH 7,4 phosphate buffer medium demonstrated a dissolution rate of 0,77 mg cm-2min-1 for NPX-TRY water slurry and 0,59 mg cm-2 min-1 for NPX-TRY ethanol slurry after 45 minutes. However, the compactibility profiles of both cocrystals were improved compared to pure naproxen.
format Final Project
author Yuliza Putri, Diana
spellingShingle Yuliza Putri, Diana
FORMULATION AND EVALUATION OF NAPROXEN AND L-TRYPTOPHAN COCRYSTAL
author_facet Yuliza Putri, Diana
author_sort Yuliza Putri, Diana
title FORMULATION AND EVALUATION OF NAPROXEN AND L-TRYPTOPHAN COCRYSTAL
title_short FORMULATION AND EVALUATION OF NAPROXEN AND L-TRYPTOPHAN COCRYSTAL
title_full FORMULATION AND EVALUATION OF NAPROXEN AND L-TRYPTOPHAN COCRYSTAL
title_fullStr FORMULATION AND EVALUATION OF NAPROXEN AND L-TRYPTOPHAN COCRYSTAL
title_full_unstemmed FORMULATION AND EVALUATION OF NAPROXEN AND L-TRYPTOPHAN COCRYSTAL
title_sort formulation and evaluation of naproxen and l-tryptophan cocrystal
url https://digilib.itb.ac.id/gdl/view/82660
_version_ 1822997781162229760