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http://dx.doi.org/10.1002/hon.3247 | DOI Listing |
ACS Appl Mater Interfaces
November 2024
Graduate Institute of Nanomedicine and Medical Engineering, College of Biomedical Engineering, Taipei Medical University, Taipei 11031, Taiwan.
Despite advancements in nanomedicine for drug delivery, many drug-loaded nanoparticles reduce tumor sizes but often fail to prevent metastasis. Mesoporous silica nanoparticles (MSNs) have attracted attention as promising nanocarriers. Here, we demonstrated that MSN-PEG/TA 25, with proper surface modifications, exhibited unique antimetastatic properties.
View Article and Find Full Text PDFJ Pharm Sci
September 2024
Arkansas Laboratory, Office of Regulatory Affairs, Office of Regulatory Science, U.S Food and Drug Administration, Jefferson, AR 72079, United States. Electronic address:
Liposomes are excellent drug delivery vehicles for chemotherapeutics as they may change the pharmacokinetics of therapeutic compounds, resulting in altered tissues distribution, and in some cases, reduced cytotoxicity and enhanced distribution and efficacy of the active pharmaceutical ingredient (API) at target tissues. Drug release profiles of liposomal formulations are crucial to support equivalence evaluation and quality control in pre- and post-approval stages. We developed an automated chromatographic method for quantifying the drug release profile of liposomal formulations containing doxorubicin to overcome the shortcomings of currently available methods.
View Article and Find Full Text PDFHematol Oncol
January 2024
Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy.
Hematol Oncol
January 2024
Department of Clinical Medicine and Surgery, Federico II University Medical School, Naples, Italy.
J Pharm Sci
March 2024
Arkansas Laboratory, Office of Regulatory Affairs, U.S. Food and Drug Administration, Jefferson, AR 72079, USA. Electronic address:
Liposomes have emerged as a drug delivery system for various chemotherapeutics providing enhanced bioavailability and reduced toxicity. In vitro drug release profiling of liposomal formulations is one of the essential tests for the premarket approval and post market quality control. We developed an automated electroanalytical method for drug release profiling of liposomal doxorubicin formulation.
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