KAJIAN PUSTAKA PSEUDOPOLIMORF OBAT ANTIVIRAL SERTA ANALISIS TRANSFORMASI HIDRAT ANTIVIRAL LAMIVUDIN DAN ASIKLOVIR

Antivirals as solid pharmaceutical ingredients can be found in their pseudopolymorphs, namely hydrates and solvates. Pseudopolymorphs affect antiviral physicochemical properties and sometimes undergo transformation because of solvents or manufacturing processes. This final project reviewed articl...

Full description

Saved in:
Bibliographic Details
Main Author: Hanifah Ismi Putri, Syimah
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/56600
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:56600
spelling id-itb.:566002021-06-23T12:42:21ZKAJIAN PUSTAKA PSEUDOPOLIMORF OBAT ANTIVIRAL SERTA ANALISIS TRANSFORMASI HIDRAT ANTIVIRAL LAMIVUDIN DAN ASIKLOVIR Hanifah Ismi Putri, Syimah Indonesia Final Project antiviral, lamivudine, acyclovir, pseudopolymorphism, hydrate, solvate. INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/56600 Antivirals as solid pharmaceutical ingredients can be found in their pseudopolymorphs, namely hydrates and solvates. Pseudopolymorphs affect antiviral physicochemical properties and sometimes undergo transformation because of solvents or manufacturing processes. This final project reviewed articles about antiviral pseudopolymorphy with stability, solubility, and dissolution rate. Several antivirals were reported in hydrates and solvates forms, that can transform to the most stable form, have various solubility, and various dissolution rates. Further experiments were carried out on lamivudine and acyclovir. This experiment was conducted to observ their pseudopolymorphs in various solvent compositions and their transformations due to thermal and mechanical processes. Lamivudin was reported as anhydrates, 1/5 hydrate, and hemihydrate forms. While acyclovir was reported as 2/3 hydrate, dihydrate, and two stable anhydrates forms. Each antiviral was recrystallized in various methanol-water compositions, then the starting material was crushed and heated at 100o C. Characterization was carried out using electrothermal, DSC, TG/DTA, FTIR, and PXRD. In this study, the starting material of lamivudine was anhydrates, its water recrystallite is 1/5 hydrate, and its methanol-water recrystallite is hemihydrate. Both recrystallites are needle-shaped. Meanwhile the starting material of acyclovir was 2/3 hydrate, its methanol recrystallite is square-shaped crystals, and its water recrystallite is needle-shaped dihydrate, with transition solvent of these two forms is 40% methanol. Crushing the two antivirals did not give significant effect on their pseudopolymorphs, meanwhile heating of acyclovir caused transformation from 2/3 hydrate to form I anhydrates. Therefore, it is necessary to pay attention during acyclovir manufacturing which gives temperature changes. 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 Antivirals as solid pharmaceutical ingredients can be found in their pseudopolymorphs, namely hydrates and solvates. Pseudopolymorphs affect antiviral physicochemical properties and sometimes undergo transformation because of solvents or manufacturing processes. This final project reviewed articles about antiviral pseudopolymorphy with stability, solubility, and dissolution rate. Several antivirals were reported in hydrates and solvates forms, that can transform to the most stable form, have various solubility, and various dissolution rates. Further experiments were carried out on lamivudine and acyclovir. This experiment was conducted to observ their pseudopolymorphs in various solvent compositions and their transformations due to thermal and mechanical processes. Lamivudin was reported as anhydrates, 1/5 hydrate, and hemihydrate forms. While acyclovir was reported as 2/3 hydrate, dihydrate, and two stable anhydrates forms. Each antiviral was recrystallized in various methanol-water compositions, then the starting material was crushed and heated at 100o C. Characterization was carried out using electrothermal, DSC, TG/DTA, FTIR, and PXRD. In this study, the starting material of lamivudine was anhydrates, its water recrystallite is 1/5 hydrate, and its methanol-water recrystallite is hemihydrate. Both recrystallites are needle-shaped. Meanwhile the starting material of acyclovir was 2/3 hydrate, its methanol recrystallite is square-shaped crystals, and its water recrystallite is needle-shaped dihydrate, with transition solvent of these two forms is 40% methanol. Crushing the two antivirals did not give significant effect on their pseudopolymorphs, meanwhile heating of acyclovir caused transformation from 2/3 hydrate to form I anhydrates. Therefore, it is necessary to pay attention during acyclovir manufacturing which gives temperature changes.
format Final Project
author Hanifah Ismi Putri, Syimah
spellingShingle Hanifah Ismi Putri, Syimah
KAJIAN PUSTAKA PSEUDOPOLIMORF OBAT ANTIVIRAL SERTA ANALISIS TRANSFORMASI HIDRAT ANTIVIRAL LAMIVUDIN DAN ASIKLOVIR
author_facet Hanifah Ismi Putri, Syimah
author_sort Hanifah Ismi Putri, Syimah
title KAJIAN PUSTAKA PSEUDOPOLIMORF OBAT ANTIVIRAL SERTA ANALISIS TRANSFORMASI HIDRAT ANTIVIRAL LAMIVUDIN DAN ASIKLOVIR
title_short KAJIAN PUSTAKA PSEUDOPOLIMORF OBAT ANTIVIRAL SERTA ANALISIS TRANSFORMASI HIDRAT ANTIVIRAL LAMIVUDIN DAN ASIKLOVIR
title_full KAJIAN PUSTAKA PSEUDOPOLIMORF OBAT ANTIVIRAL SERTA ANALISIS TRANSFORMASI HIDRAT ANTIVIRAL LAMIVUDIN DAN ASIKLOVIR
title_fullStr KAJIAN PUSTAKA PSEUDOPOLIMORF OBAT ANTIVIRAL SERTA ANALISIS TRANSFORMASI HIDRAT ANTIVIRAL LAMIVUDIN DAN ASIKLOVIR
title_full_unstemmed KAJIAN PUSTAKA PSEUDOPOLIMORF OBAT ANTIVIRAL SERTA ANALISIS TRANSFORMASI HIDRAT ANTIVIRAL LAMIVUDIN DAN ASIKLOVIR
title_sort kajian pustaka pseudopolimorf obat antiviral serta analisis transformasi hidrat antiviral lamivudin dan asiklovir
url https://digilib.itb.ac.id/gdl/view/56600
_version_ 1822930245856002048