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   <subfield code="a">​​​​UPPharm</subfield>
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   <subfield code="a">eng</subfield>
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   <subfield code="a">Arcenas, Ma. Giselle D.​</subfield>
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   <subfield code="a">Optimization of clopidogrel nanoparticles formulation by Jassim &amp; Hussein, 2014 using polyvinyl alcohol (PVA) &amp; polyvinylpyrrolidone (PVP) K30</subfield>
   <subfield code="c">Ma. Giselle D. Arcenas, Mary Lord Sheehan B. Olinares, Cleo P. Valiente ; adviser, Jean Flor C. Casauay ; co-adviser, Clinton B. Gomez.</subfield>
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   <subfield code="a">Manila</subfield>
   <subfield code="b">College of Pharmacy, University of the Philippines</subfield>
   <subfield code="c">2019.</subfield>
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   <subfield code="a">49 leaves</subfield>
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   <subfield code="2">rdacarrier</subfield>
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   <subfield code="a">​Thesis (Bachelor of Science in Industrial Pharmacy)--University of the Philippines, June 2019.</subfield>
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   <subfield code="a">Yes - available to the general public.</subfield>
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   <subfield code="a">The study aims to optimize clopidogrel nanoparticles formulated by Jassim and Hussein (2014) using a combination of PVA and PVP K30 polymers as stabilizers with modifications on the size of the needle gauge and stirring speed. Clopidogrel nanoparticles were produced via antisolvent-precipitation method at drug:stabilizer ratio of 1:1, 1:2 and 1:4 and at stabilizer:stabilizer ratio of 2:1, 1:1 and 1:2. The formulated clopidogrel nanoparticles were characterized for surface morphology, particle size distribution, zeta potential, drug encapsulation efficiency, in vitro dissolution and drug-stabilizer compatibility.</subfield>
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   <subfield code="a">All resulting nanosuspensions (F1 to F9) appeared as clear solutions with water-like consistency and with absence of agglomerations. SEM of clopidogrel nanoparticles confirmed relatively spherical in shape and surface which varies from rough to smooth. F8 showed a monodisperse distribution in dynamic light scattering with an average size and polydispersity index of 816.3 nm and 0.505, respectively. F5 has the most ideal zeta potential (-33.180 mV), F4 has the highest drug entrapment efficiency (99.5843%), and F9 has the highest in-vitro drug release (13.0381%). FTIR study also revealed that there is no chemical interaction between clopidogrel and the stabilizers.</subfield>
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   <subfield code="a">Clopidogrel nanoparticles were successfully formulated using Jassim and Hussein?s (2014) anti-solvent precipitation method with modifications on needle gauge size (26G) and stirring speed (1000 rpm). However, further testing should be done, particularly on the particle size distribution, to determine the optimum clopidogrel nanoparticles formulation.</subfield>
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   <subfield code="a">Clopidogrel.</subfield>
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   <subfield code="a">Nanoparticles.</subfield>
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   <subfield code="a">Polyvinyl alcohol.</subfield>
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   <subfield code="a">Povidone.</subfield>
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   <subfield code="a">Olinares, Mary Lord Sheehan B.​</subfield>
   <subfield code="e">author.</subfield>
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   <subfield code="a">Valiente, Cleo P.​</subfield>
   <subfield code="e">author.</subfield>
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   <subfield code="a">Casauay, Jean Flor C.​</subfield>
   <subfield code="e">thesis adviser.</subfield>
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   <subfield code="a">Gomez, Clinton B.​</subfield>
   <subfield code="e">thesis co-adviser.</subfield>
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