Dosage Form Design Considerations 2018
DOI: 10.1016/b978-0-12-814423-7.00010-1
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Drug Disposition Considerations in Pharmaceutical Product

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Cited by 4 publications
(3 citation statements)
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“…[66] As key organs of the MPS, the liver and spleen contain macrophages (Kupffer cells and splenic macrophages, respectively), which seem to play a major role in phage degradation, with the initial phagocytic activity of Kupffer cells in the liver being more effective than splenic macrophages at inactivating phage. [58,70] Phage inactivation by the liver and spleen are observed to differ, with phage degradation occurring at a slower rate in the spleen. [53,58,63] Longer half-lives of phage in spleen compared to the liver and recovery of intact phage up to 7 days post-injection from the spleen also indicate that the spleen acts as a "phage sink."…”
Section: Phage Biodistributionmentioning
confidence: 99%
“…[66] As key organs of the MPS, the liver and spleen contain macrophages (Kupffer cells and splenic macrophages, respectively), which seem to play a major role in phage degradation, with the initial phagocytic activity of Kupffer cells in the liver being more effective than splenic macrophages at inactivating phage. [58,70] Phage inactivation by the liver and spleen are observed to differ, with phage degradation occurring at a slower rate in the spleen. [53,58,63] Longer half-lives of phage in spleen compared to the liver and recovery of intact phage up to 7 days post-injection from the spleen also indicate that the spleen acts as a "phage sink."…”
Section: Phage Biodistributionmentioning
confidence: 99%
“…The treatment of cancers and diseases is a key area of application for these innovative sustained-release systems. Biopolymer delivery capabilities require drugs to be prescribed periodically when treating hormone disorders and geriatric diseases [ 110 , 111 ].…”
Section: Applications Of Different Polysaccharidesmentioning
confidence: 99%
“…Hence, great care must be taken in the delicate process of sedation management ( 14 ), where patients may exhibit unique pharmacological responses for the same dose of a given medication. This results in pharmacokinetic or pharmacodynamic variations for the same drug administered with the same frequency in different individuals ( 18 , 19 ). In order to address this issue, a growing number of clinical studies have proposed automated methods based on patients' evolving clinical phenotypes to deliver safe and effective sedation regulation ( 6 , 16 , 20 ).…”
Section: Introductionmentioning
confidence: 99%