Development of supramolecular anticoagulants with on-demand reversibility.

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Tác giả: Imala Alwis, Simona Angerani, Millicent Dockerill, Luke J Dowman, Daniel J Ford, Shaun P Jackson, Joanna S T Liu, Richard J Payne, Pedro José Barbosa Pereira, Jorge Ripoll-Rozada, Rhyll E Smythe, Nicolas Winssinger

Ngôn ngữ: eng

Ký hiệu phân loại: 784.1886 General principles, musical forms, instruments

Thông tin xuất bản: United States : Nature biotechnology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 59215

Drugs are administered at a dosing schedule set by their therapeutic index, and termination of action is achieved by clearance and metabolism of the drug. In some cases, such as anticoagulant drugs or immunotherapeutics, it is important to be able to quickly reverse the drug's action. Here, we report a general strategy to achieve on-demand reversibility by designing a supramolecular drug (a noncovalent assembly of two cooperatively interacting drug fragments held together by transient hybridization of peptide nucleic acid (PNA)) that can be reversed with a PNA antidote that outcompetes the hybridization between the fragments. We demonstrate the approach with thrombin-inhibiting anticoagulants, creating very potent and reversible bivalent direct thrombin inhibitors (K
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