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<title><![CDATA[Peningkatan Laju Disolusi Acyclovir Dengan Metode Sistem Dispersi Padat Menggunakan Poloxamer 188]]></title>
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<namePart>Budi Setiawan</namePart>
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<publisher><![CDATA[SCIENTIA]]></publisher>
<dateIssued><![CDATA[2015]]></dateIssued>
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<languageTerm type="text"><![CDATA[Indonesia]]></languageTerm>
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<note>A study on the solid dispersion system of Acyclovir with poloxamer 188 has been conducted a physical mixture formulation with a ratio of 1 : 1, 1 : 3, 1 : 5 and solid dispersion 1 : 1, 1 : 3, 1 : 5 and cogrinding 1 : 1 as a comparison. Solid dispersions made by the method of melting (fusion), which merged with poloxamer 188 on the hot plate then acyclovir incorporated into the fused results in poloxamer 188 while stirring to form a homogeneous mass. All formulas are formed including poloxamer 188 acyclovir pure and good analysis that test kerakterisasi with Differential Thermal Analysis (DTA), X-ray Diffraction, Scanning Electron Microscopy (SEM), and Fourier Transform Infrared (FTIR), then performed retrieval (determination levels) by UV spectrophotometry at a wavelength of 257.08 nm and dissolution rate test with CO2-free aquadest using the paddle method. Retrieval results (determination of Kedar) found that all formulas meet the requirements set forth in United States Pharmacopeia 30, and the fourth edition of the Pharmacopoeia Indonesia 95-110%. While the dissolution rate test results for a physical mixture of 1 : 1, and solid dispersion 1 : 1, and co-grinding 1 : 1 experienced a significant increase when compared with pure Acyclovir. It also can be seen from the results of the statistical calculations using one-way analysis of variance SPSS 17</note>
<subject authority=""><topic><![CDATA[Peningkatan Laju Disolusi Acyclovir]]></topic></subject>
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