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Loftsson, Cyclodextrins in Parenteral Formulations, Journal of Pharmaceutical Sciences, 2020, 1-11], Their hydrophobic microenvironment inside the cavity of these cone-like structures enables them to form drug-to-cyclodextrin complexes mainly through hydrophobic interactions [T
Structural Protein Pathways: Examined in models related to collagen-associated processes
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doi: 10.1016/j.medcle.2018.09.013 432 SunKLiuZWangH
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