Опубликована: Янв. 1, 2024
Язык: Английский
Опубликована: Янв. 1, 2024
Язык: Английский
International Journal of Pharmaceutics, Год журнала: 2024, Номер unknown, С. 124869 - 124869
Опубликована: Окт. 1, 2024
Язык: Английский
Процитировано
4Journal of Molecular Liquids, Год журнала: 2024, Номер unknown, С. 126541 - 126541
Опубликована: Ноя. 1, 2024
Язык: Английский
Процитировано
4npj Vaccines, Год журнала: 2025, Номер 10(1)
Опубликована: Янв. 3, 2025
Язык: Английский
Процитировано
0International Journal of Pharmaceutics, Год журнала: 2025, Номер unknown, С. 125247 - 125247
Опубликована: Янв. 1, 2025
Язык: Английский
Процитировано
0Small, Год журнала: 2025, Номер unknown
Опубликована: Март 27, 2025
Proteins are typically subject to poor stability, short half-life, and cell tissue permeability, which restrict their wide applications as drugs for disease treatment. Current protein modification techniques mostly focus on improving the stability half-life of proteins, but hardly solve permeability. To address this issue, study innovatively designs thermo-pH-sensitive elastin-like polypeptides modify named ELP(HX)n in histidine (H) any amino acid except proline (X) guest acids n is total number acids. H can be protonated under acidic conditions. prove concept, an important drug L-asparaginase (ASP) genetically fused ELP(HV)60 generate ASP-ELP(HV)60. Compared with ASP PEGylated ASP, ASP-ELP(HV)60 exhibits not only elevated extended also enhanced tumor penetration, resulting improved antitumor efficacy. These findings demonstrate that fusion a novel general method overcome intrinsic limitations proteins therapeutics, rendering it feasible design intelligent especially efficient therapy.
Язык: Английский
Процитировано
0Journal of Drug Delivery Science and Technology, Год журнала: 2025, Номер unknown, С. 106947 - 106947
Опубликована: Апрель 1, 2025
Язык: Английский
Процитировано
0Acta Biomaterialia, Год журнала: 2024, Номер 189, С. 25 - 56
Опубликована: Сен. 20, 2024
Язык: Английский
Процитировано
3Journal of Molecular Structure, Год журнала: 2024, Номер 1315, С. 138618 - 138618
Опубликована: Май 14, 2024
Язык: Английский
Процитировано
2AAPS PharmSciTech, Год журнала: 2024, Номер 25(7)
Опубликована: Сен. 5, 2024
Язык: Английский
Процитировано
2Опубликована: Июнь 20, 2024
Nanovaccines are able to deliver antigen(s) and immunomodulator(s) directly antigen-presenting cells (APCs) of the lymphatic system. Positive charges improve their uptake by APCs often drive a Th-1 biased immune response so necessary against infectious diseases caused intracellular pathogens cancers. However, cationic compounds display dose-dependent toxicity that systematic evaluation cytotoxicity in culture is required. After rapid evolution nanovaccines SARS-Covid 2, mRNA vaccines gained much strength have been designed several diseases, relying on components for protection. Once established limiting concentration compound, perform well eliciting desired improved most cases. Other valuable approach found literature has construction biocompatible nanoparticles (NPs) carrying lipids, polymers or surfactants minimization component led absence toxicity. Against cancer, recent constructions situ after cancer cell disruption presence adjuvants systemic presentation multiple tumoral antigens yielding, many instances, prevention metastasis appearance conversion tumors non treatable immunotherapy into ones.
Язык: Английский
Процитировано
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