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The drug release is dependent on time and temperature, making it ideal for applications involving hyperthermia.
It was found that N-Ac-Tyr-OEt release is dependent on TK concentration (U/mL) in the electrolyte medium.
However, the duration of release is dependent on the amount of protein loaded and the bioactive molecules in the coating; that is, it is limited.
The BSA release as a function of time became less rapid as the CFCA-Ap particles were immersed in higher pH solution, thus indicating that the BSA release is dependent on the local pH.
From these results, we can conclude that the release of incorporated DNA from polymeric micelles/DNA complexes is triggered by the reductive cleavage of disulfide bond in the polymer main chain and the rate of DNA release is dependent on the DTT concentration.
We demonstrate that depolarization of these cells leads to NO-release and that this release is dependent on the presence of functional endothelial NO-synthase.
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Paclitaxel release was dependent on the enzyme concentration.
HMGB1 induction of proinflammatory cytokines interleukin (IL -1β and IL -1βreleand was dependent on ER stress.
The release was dependent on the nature of the adsorbent used to prepare the complexes.
Results showed the matrix erosion rate and drug release were dependent on HPMC content and drug solubility, as expected.
The optical properties and efficiency of photo-induced NO release were dependent upon the nature of the conjugation system.
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