FORMULASI DAN KARAKTERISASI NANOKARIER ARTEMISININ SERTA UJI AKTIVITAS ANTIMALARIA DARI SEDIAAN SECARA IN VITRO

Malaria treatment failure may be caused by the low bioavailability of the drugs and nonspecific drug targets to intracellular parasites. Artemisinin as a first-line treatment of malaria have limitations such as hydrophobicity, a short half-life and low bioavailability resulting in a low therapeuti...

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Main Author: Elisabeth E Haloho, Sion
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/45383
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:45383
spelling id-itb.:453832019-12-18T11:16:41ZFORMULASI DAN KARAKTERISASI NANOKARIER ARTEMISININ SERTA UJI AKTIVITAS ANTIMALARIA DARI SEDIAAN SECARA IN VITRO Elisabeth E Haloho, Sion Indonesia Final Project artemisinin, nanocarrier, PLGA-poloxamer INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/45383 Malaria treatment failure may be caused by the low bioavailability of the drugs and nonspecific drug targets to intracellular parasites. Artemisinin as a first-line treatment of malaria have limitations such as hydrophobicity, a short half-life and low bioavailability resulting in a low therapeutic effectiveness. To improve the effectiveness of therapy, antimalarial delivery systems need to be made selective towards red blood cells infected with parasites. Because of it, nanocarrier consist of PLGA-poloxamer as artemisinin delivery system was developed. Nanocarrier was developed with nanopresipitation method. Nanocarrier formula was made by 5% poloxamer and varied concentration of PLGA. Characterization of dosage form includes a physical characterization of particle size, polydispersity index and a visual display. Chemical characterizations include encapsulation efficiency and in vitro release test. Antimalarial activity test preparation performed on culture conditions parasite Plasmodium falciparum 3D7 dominant phase of the ring. Observations were made on the preparations layer of thick blood of the test results by counting the number parasite in schizont phase and total asexual plasmodium. Nanocarrier particle size increased with increasing concentrations of PLGA polymer. Encapsulation efficiancy increased with increasing concentration of PLGA polymers. In vitro release test at pH 7.4 and pH 5.5 showed no considerable difference in the testing of formulas with different concentrations of PLGA. Antimalarial activity in vitro assay for formula PLGA 1 %, poloxamer 5% with artemisinin concentration 10 ppm, provided 43.65 ± 8.5284% of inhibition percent. Artemisinin standard of 10 ppm without nanocarrier delivery systems provided 27 833 ± 0.0288% (p <0.05) of percent inhibition. Nanocarrier formula of artemisinin with artemisinin concentration of 10 ppm, 5% poloxamer, and 1.0% PLGA give a better activity than the standard without nanocarrier system. 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 Malaria treatment failure may be caused by the low bioavailability of the drugs and nonspecific drug targets to intracellular parasites. Artemisinin as a first-line treatment of malaria have limitations such as hydrophobicity, a short half-life and low bioavailability resulting in a low therapeutic effectiveness. To improve the effectiveness of therapy, antimalarial delivery systems need to be made selective towards red blood cells infected with parasites. Because of it, nanocarrier consist of PLGA-poloxamer as artemisinin delivery system was developed. Nanocarrier was developed with nanopresipitation method. Nanocarrier formula was made by 5% poloxamer and varied concentration of PLGA. Characterization of dosage form includes a physical characterization of particle size, polydispersity index and a visual display. Chemical characterizations include encapsulation efficiency and in vitro release test. Antimalarial activity test preparation performed on culture conditions parasite Plasmodium falciparum 3D7 dominant phase of the ring. Observations were made on the preparations layer of thick blood of the test results by counting the number parasite in schizont phase and total asexual plasmodium. Nanocarrier particle size increased with increasing concentrations of PLGA polymer. Encapsulation efficiancy increased with increasing concentration of PLGA polymers. In vitro release test at pH 7.4 and pH 5.5 showed no considerable difference in the testing of formulas with different concentrations of PLGA. Antimalarial activity in vitro assay for formula PLGA 1 %, poloxamer 5% with artemisinin concentration 10 ppm, provided 43.65 ± 8.5284% of inhibition percent. Artemisinin standard of 10 ppm without nanocarrier delivery systems provided 27 833 ± 0.0288% (p <0.05) of percent inhibition. Nanocarrier formula of artemisinin with artemisinin concentration of 10 ppm, 5% poloxamer, and 1.0% PLGA give a better activity than the standard without nanocarrier system.
format Final Project
author Elisabeth E Haloho, Sion
spellingShingle Elisabeth E Haloho, Sion
FORMULASI DAN KARAKTERISASI NANOKARIER ARTEMISININ SERTA UJI AKTIVITAS ANTIMALARIA DARI SEDIAAN SECARA IN VITRO
author_facet Elisabeth E Haloho, Sion
author_sort Elisabeth E Haloho, Sion
title FORMULASI DAN KARAKTERISASI NANOKARIER ARTEMISININ SERTA UJI AKTIVITAS ANTIMALARIA DARI SEDIAAN SECARA IN VITRO
title_short FORMULASI DAN KARAKTERISASI NANOKARIER ARTEMISININ SERTA UJI AKTIVITAS ANTIMALARIA DARI SEDIAAN SECARA IN VITRO
title_full FORMULASI DAN KARAKTERISASI NANOKARIER ARTEMISININ SERTA UJI AKTIVITAS ANTIMALARIA DARI SEDIAAN SECARA IN VITRO
title_fullStr FORMULASI DAN KARAKTERISASI NANOKARIER ARTEMISININ SERTA UJI AKTIVITAS ANTIMALARIA DARI SEDIAAN SECARA IN VITRO
title_full_unstemmed FORMULASI DAN KARAKTERISASI NANOKARIER ARTEMISININ SERTA UJI AKTIVITAS ANTIMALARIA DARI SEDIAAN SECARA IN VITRO
title_sort formulasi dan karakterisasi nanokarier artemisinin serta uji aktivitas antimalaria dari sediaan secara in vitro
url https://digilib.itb.ac.id/gdl/view/45383
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