Drug Loading in Poly(butyl cyanoacrylate)-Based Polymeric Microbubbles.
Drug Loading in Poly(butyl cyanoacrylate)-Based Polymeric Microbubbles.
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DOI:
10.1021/acs.molpharmaceut.0c00242
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发表时间:
2020-08-03
影响因子:
4.9
通讯作者:
Lammers T
中科院分区:
文献类型:
--
作者:
Liu M;Dasgupta A;Koczera P;Schipper S;Rommel D;Shi Y;Kiessling F;Lammers T
Microbubbles (MB) are routinely used ultrasound (US) contrast agents that have recently attracted increasing attention as stimuli-responsive drug delivery systems. In order to better understand MB-based drug delivery, we studied the role of drug hydrophobicity and molecular weight on MB loading, shelf-life stability, US properties and drug release. Eight model drugs, varying in hydrophobicity and molecular weight, were loaded into the shell of poly(butyl cyanoacrylate) (PBCA) MB. In the case of drugs with progesterone as a common structural backbone (i.e. for corticosteroids), loading capacity and drug release correlated well with hydrophobicity and molecular weight. Conversely, when employing drugs with no structural similarity (i.e. four different fluorescent dyes), loading capacity and release did not correlate with hydrophobicity and molecular weight. All model drug-loaded MB formulations could be equally efficiently destroyed upon exposure to US. Together, these findings provide valuable insights on how the physicochemical properties of (model) drug molecules affect their loading and retention in and US-induced release from polymeric MB, thereby facilitating the development of drug-loaded MB formulations for US-triggered drug delivery.
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DOI:
10.1179/175889709x446507
发表时间:
2009-11
期刊:
Bubble science engineering and technology
影响因子:
--
作者:
Sirsi S;Borden M
通讯作者:
Borden M
影响因子:
10.8
作者:
Koczera, Patrick;Appold, Lia;Lammers, Twan
通讯作者:
Lammers, Twan
影响因子:
6.4
作者:
Treat, Lisa H.;McDannold, Nathan;Hynynen, Kullervo
通讯作者:
Hynynen, Kullervo
影响因子:
4.9
作者:
Liu, Zhe;Koczera, Patrick;Gaetjens, Jessica
通讯作者:
Gaetjens, Jessica
影响因子:
6.7
作者:
Wan, Yiqun;Wang, Xiaofen;Xu, Zhaodi
通讯作者:
Xu, Zhaodi