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  • Influence of different formulations and process parameters during the preparation of drug-loaded PLGA microspheres evaluated by multivariate data analysis.

Influence of different formulations and process parameters during the preparation of drug-loaded PLGA microspheres evaluated by multivariate data analysis.

Acta pharmaceutica (Zagreb, Croatia) (2014-12-23)
Jakub Vysloužil, Petr Doležel, Martina Kejdušová, Eliška Mašková, Josef Mašek, Robert Lukáč, Vratislav Košťál, David Vetchý, Kateřina Dvořáčková
ABSTRACT

The main objective of this study was to evaluate the influence of the formulation and process parameters on PLGA microparticles containing a practically insoluble model drug (ibuprofen) prepared by the o/w solvent evaporation method. Multivariate data analysis was used. The effects of altered stirring speed of a mechanical stirrer (600, 1000 rpm), emulsifier concentrations (PVA concentration 0.1 %, 1 %) and solvent selection (dichloromethane, ethyl acetate) on microparticle characteristics (encapsulation efficiency, drug loading, burst effect) were observed. It was found that with increased stirring speed, the PVA concentration or the use of ethyl acetate had a significantly negative effect on encapsulation efficiency. In addition, ethyl acetate had an adverse effect on the burst effect, while increased stirring speed had the opposite effect. Drug load was not affected by any particular variable, but rather by the interactions of evaluated variables.

MATERIALS
Product Number
Brand
Product Description

Supelco
Phosphate Standard for IC, TraceCERT®, 1000 mg/L phosphate in water (nominal concentration)
Supelco
Ibuprofen, Pharmaceutical Secondary Standard; Certified Reference Material
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Ibuprofen
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Ibuprofen, ≥98% (GC)
Ibuprofen, European Pharmacopoeia (EP) Reference Standard
Ibuprofen for peak identification, European Pharmacopoeia (EP) Reference Standard
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Ibuprofen, meets USP testing specifications
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Sodium phosphate dibasic solution, BioUltra, 0.5 M in H2O
USP
Ibuprofen, United States Pharmacopeia (USP) Reference Standard
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Dichloromethane, suitable for HPLC, ≥99.9%, contains 40-150 ppm amylene as stabilizer
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Sodium phosphate dibasic, purum p.a., anhydrous, ≥98.0% (T)
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Dichloromethane, analytical standard
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Potassium phosphate monobasic, tested according to Ph. Eur., anhydrous
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Dichloromethane, Selectophore, ≥99.5%
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Potassium phosphate monobasic, 99.99% trace metals basis
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Sodium phosphate dibasic, BioUltra, for molecular biology, ≥99.5% (T)
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Sodium phosphate dibasic, ReagentPlus®, ≥99.0%
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Potassium phosphate monobasic, powder, suitable for cell culture, suitable for insect cell culture, suitable for plant cell culture, ≥99.0%
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Sodium phosphate dibasic, BioReagent, suitable for cell culture, suitable for insect cell culture, ≥99.0%
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Monobasic Potassium Phosphate, Pharmaceutical Secondary Standard; Certified Reference Material
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Potassium phosphate monobasic, BioUltra, for molecular biology, anhydrous, ≥99.5% (T)
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Potassium phosphate monobasic, ACS reagent, ≥99.0%
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Dichloromethane, suitable for HPLC, ≥99.8%, contains amylene as stabilizer
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Dichloromethane, HPLC Plus, for HPLC, GC, and residue analysis, ≥99.9%, contains 50-150 ppm amylene as stabilizer
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Sodium phosphate dibasic, puriss. p.a., ACS reagent, anhydrous, ≥99.0% (T)