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Journal Abstract Search
675 related items for PubMed ID: 27112112
1. Mechanism and kinetics of the loss of poorly soluble drugs from liposomal carriers studied by a novel flow field-flow fractionation-based drug release-/transfer-assay. Hinna AH, Hupfeld S, Kuntsche J, Bauer-Brandl A, Brandl M. J Control Release; 2016 Jun 28; 232():228-37. PubMed ID: 27112112 [Abstract] [Full Text] [Related]
2. The use of asymmetrical flow field-flow fractionation with on-line detection in the study of drug retention within liposomal nanocarriers and drug transfer kinetics. Hinna AH, Hupfeld S, Kuntsche J, Brandl M. J Pharm Biomed Anal; 2016 May 30; 124():157-163. PubMed ID: 26950903 [Abstract] [Full Text] [Related]
3. Asymmetrical flow field-flow fractionation with on-line detection for drug transfer studies: a feasibility study. Hinna A, Steiniger F, Hupfeld S, Brandl M, Kuntsche J. Anal Bioanal Chem; 2014 Dec 30; 406(30):7827-39. PubMed ID: 24518901 [Abstract] [Full Text] [Related]
4. Application of Asymmetrical Flow Field-Flow Fractionation for Characterizing the Size and Drug Release Kinetics of Theranostic Lipid Nanovesicles. Skupin-Mrugalska P, Elvang PA, Brandl M. Int J Mol Sci; 2021 Sep 28; 22(19):. PubMed ID: 34638795 [Abstract] [Full Text] [Related]
5. Pharmacokinetics of temoporfin-loaded liposome formulations: correlation of liposome and temoporfin blood concentration. Decker C, Schubert H, May S, Fahr A. J Control Release; 2013 Mar 28; 166(3):277-85. PubMed ID: 23313962 [Abstract] [Full Text] [Related]
6. Investigations of the influence of liposome composition on vesicle stability and drug transfer in human plasma: a transfer study. Holzschuh S, Kaeß K, Bossa GV, Decker C, Fahr A, May S. J Liposome Res; 2018 Mar 28; 28(1):22-34. PubMed ID: 27750473 [Abstract] [Full Text] [Related]
7. Transfer mechanism of temoporfin between liposomal membranes. Hefesha H, Loew S, Liu X, May S, Fahr A. J Control Release; 2011 Mar 30; 150(3):279-86. PubMed ID: 20888878 [Abstract] [Full Text] [Related]
15. Liposome transport of hydrophobic drugs: gel phase lipid bilayer permeability and partitioning of the lactone form of a hydrophobic camptothecin, DB-67. Joguparthi V, Xiang TX, Anderson BD. J Pharm Sci; 2008 Jan 10; 97(1):400-20. PubMed ID: 17879989 [Abstract] [Full Text] [Related]