2020
DOI: 10.3390/pharmaceutics12050433
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Physicochemical Properties of Poly-vinyl Polymers and Their Influence on Ketoprofen Amorphous Solid Dispersion Performance: A Polymer Selection Case Study

Abstract: When developing an amorphous solid dispersion (ASD), a prudent choice of polymer is critical to several aspects of ASD performance including: processability, solid state stability and dissolution rate. However, there is little guidance available to formulators to aid judicious polymer selection and a “trial and error” approach is often taken. This study aims to facilitate rational polymer selection and formulation design by generating ASDs using a range of poly-vinyl polymers and ketoprofen as a model active p… Show more

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Cited by 49 publications
(36 citation statements)
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“…The increase in molecular weight of PVP has shown the reduction of nucleation and crystal growth of piroxicam (Hilton & Summers, 1986 ). The high molecular weight polymer may give slow drug release from the SDs due to high viscosity of the diffusion layer (Browne et al., 2020 ).…”
Section: Selection Of Polymermentioning
confidence: 99%
“…The increase in molecular weight of PVP has shown the reduction of nucleation and crystal growth of piroxicam (Hilton & Summers, 1986 ). The high molecular weight polymer may give slow drug release from the SDs due to high viscosity of the diffusion layer (Browne et al., 2020 ).…”
Section: Selection Of Polymermentioning
confidence: 99%
“…The sole PLGA in the oil phase, together with lecithin and maltose in the water phase, brought to the formation of big pores, but such pores had a closed morphology. The addition of PVP/VA in the oil phase allowed to obtain microneedles with an interconnected porosity, where the polymer chains of PVP, being PVP hydrophilic, were entrapped together with the drug (Browne et al 2020 ). These microneedle microstructure and porosity are related to the amount of drug that can be loaded inside the polymeric matrix and to the MN release rate.…”
Section: Discussionmentioning
confidence: 99%
“…The degree to which the drug and carriers are miscible strongly affects the solubility characteristics of the SD system [ 37 ]. Therefore, in order to derive the maximum solubility advantages from the solid dispersion system, impart a stronger drug–carrier interaction at molecular level, and prepare a stable SD system, the judicious selection of carriers is crucial.…”
Section: Resultsmentioning
confidence: 99%