HPBCD against acute and subacute infarcts in a mouse model of ischemic stroke
HPβCD has also been investigated as an active pharmaceutical ingredient (API) for the prospective treatment of ischemic stroke. We previously
A forum for researchers, students and applicants in the field of cyclodextrin technology
HPβCD has also been investigated as an active pharmaceutical ingredient (API) for the prospective treatment of ischemic stroke. We previously
For years, oat milk has been one of the most successful plant-based dairy alternatives, winning over consumers with its creamy
Cyclodextrin-based metal-organic frameworks (CD-MOFs) constitute a distinctive family of porous solids that combine the modularity of coordination networks with the
HPβCD has also been investigated as an active pharmaceutical ingredient (API) for the prospective treatment of ischemic stroke. We previously
This thematic issue in Beilstein Journal of Organic Chemistry aims at collecting new discovies on macrocycles such as cucurbiturils, calixarenes,
For years, oat milk has been one of the most successful plant-based dairy alternatives, winning over consumers with its creamy
Cyclodextrin-based metal-organic frameworks (CD-MOFs) constitute a distinctive family of porous solids that combine the modularity of coordination networks with the
3D cyclodextrin-based metal-organic frameworks (CD-MOFs) have emerged as a biocompatible alternative to conventional MOFs, as they are synthesized using safer,
In this work, an integrated biophysical and biological study is presented describing both the structural and biological features of the
The 2nd International Conference on Biomedical Science and Engineering will be held on June 22-23, 2026 in London. Conference Sessions
Compared with neostigmine, sugammadex promotes faster neuromuscular recovery, but its impact on diaphragmatic function and respiratory recovery in the morbidly
The scope of this review is to provide a comprehensive overview of the current synthetic methodologies for both mono- and
The comprehensive physicochemical characterization and cyclodextrin complexation of four tyrosine kinase inhibitors — erlotinib, gefitinib, vandetanib, and lapatinib — were