A systematic evaluation of the cucurbit[7]uril pharmacokinetics and toxicity after a single dose and short-term repeated administration in mice
Author:
Funder
Grantová Agentura České Republiky
Publisher
Springer Science and Business Media LLC
Subject
Health, Toxicology and Mutagenesis,Toxicology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00204-022-03249-7.pdf
Reference38 articles.
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2. Andrys R, Klusonova A, Lisa M, Kassa J, Zdarova Karasova J (2021) Effect of oxime encapsulation on acetylcholinesterase reactivation: pharmacokinetic study of the asoxime–cucurbit[7]uril complex in mice using hydrophilic interaction liquid chromatography-mass spectrometry. Mol Pharm 18(6):2416–2427. https://doi.org/10.1021/acs.molpharmaceut.1c00257
3. Brewster ME, Loftsson T (2007) Cyclodextrins as pharmaceutical solubilizers. Adv Drug Delivery Rev 5:645–666. https://doi.org/10.1016/j.addr.2007.05.012
4. Brewster ME, Loftsson T (2010) Pharmaceutical applications of cyclodextrins: basic science and product development. J Pharm Pharmacol 62(11):1607–1621. https://doi.org/10.1111/j.2042-7158.2010.01030.x
5. Carvalho CP, Uzunova VD, Da Silva JP, Nau WM, Pischel U (2011) A photoinduced pH jump applied to drug release from cucurbit[7]uril. Chem Commun (camb) 47(31):8793–8795. https://doi.org/10.1039/c1cc12954f
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