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In vitro/vivo assessment of praziquantel nanocrystals: Formulation, characterization, and pharmacokinetics in beagle dogs 被引量:1

In vitro/vivo assessment of praziquantel nanocrystals: Formulation, characterization, and pharmacokinetics in beagle dogs
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摘要 To investigate the impact of particle size on in vitro/vivo performance of praziquantel(PZQ), nanocrystals(NCs) and microcrystals(MCs) of PZQ were prepared using the methods of wet milling and jet milling, respectively. PZQ NCs and MCs were characterized with dynamic light scattering, laser particle size analyzer, transmission electron microscopy, differential scanning calorimetry, X-ray powder diffraction and fourier transform infrared spectroscopy. The average diameters of PZQ NCs and MCs were 364.4 nm and 3.7 μm, respectively. No change in crystalline form was observed. Dissolution tests were performed in two different media, where the cumulative dissolution and dissolution rate of NCs were significantly improved in comparison with those of MCs and KANGQING~? in non-sink condition. Similarly, oral bioavailability of PZQ NCs in beagle dogs was 1.68( P < 0.05) and 1.83 fold( P < 0.01) higher than that of MCs and KANGQING~? . Considering the advantages of in vitro/vivo performance and facile preparation, PZQ NCs may have a great application in the treatment of schistosomiasis. To investigate the impact of particle size on in vitro/vivo performance of praziquantel(PZQ), nanocrystals(NCs) and microcrystals(MCs) of PZQ were prepared using the methods of wet milling and jet milling, respectively. PZQ NCs and MCs were characterized with dynamic light scattering, laser particle size analyzer, transmission electron microscopy, differential scanning calorimetry, X-ray powder diffraction and fourier transform infrared spectroscopy. The average diameters of PZQ NCs and MCs were 364.4 nm and 3.7 μm, respectively. No change in crystalline form was observed. Dissolution tests were performed in two different media, where the cumulative dissolution and dissolution rate of NCs were significantly improved in comparison with those of MCs and KANGQING~? in non-sink condition. Similarly, oral bioavailability of PZQ NCs in beagle dogs was 1.68( P < 0.05) and 1.83 fold( P < 0.01) higher than that of MCs and KANGQING~? . Considering the advantages of in vitro/vivo performance and facile preparation, PZQ NCs may have a great application in the treatment of schistosomiasis.
出处 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2019年第3期321-328,共8页 亚洲药物制剂科学(英文)
关键词 PRAZIQUANTEL NANOCRYSTALS MICROCRYSTALS DISSOLUTION PHARMACOKINETICS Praziquantel Nanocrystals Microcrystals Dissolution Pharmacokinetics
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