2017
DOI: 10.1007/s10934-017-0538-3
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The synergistic cooperation between MCM-41 and azithromycin: a pH responsive system for drug adsorption and release

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Cited by 17 publications
(6 citation statements)
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“…Clearly, the pH of the solution greatly influenced the adsorption process of macrolide antibiotics, and the uptake of AZM and ROX was increased from 0.67 mg/g to 36.69 mg/g and 16.59 mg/g to 49.04 mg/g, respectively, when pH increased from 3.0 to 13.0. This situation was consistent with the conclusions of a previous study [35]. As a result, the adsorption capacity of 6 h-synthesized zeolite EMANA is low at low pH values, specifically below 5, due to electrostatic repulsion between macrolide antibiotics and 6 h-synthesized zeolite EMANA.…”
Section: Resultssupporting
confidence: 93%
“…Clearly, the pH of the solution greatly influenced the adsorption process of macrolide antibiotics, and the uptake of AZM and ROX was increased from 0.67 mg/g to 36.69 mg/g and 16.59 mg/g to 49.04 mg/g, respectively, when pH increased from 3.0 to 13.0. This situation was consistent with the conclusions of a previous study [35]. As a result, the adsorption capacity of 6 h-synthesized zeolite EMANA is low at low pH values, specifically below 5, due to electrostatic repulsion between macrolide antibiotics and 6 h-synthesized zeolite EMANA.…”
Section: Resultssupporting
confidence: 93%
“…The mechanism of 5-FU in-vitro release from SBA-15_N-ANI_5-FU_β-CD system was also studied from a kinetic point of view. In general, the release kinetics of drugs from ordered mesoporous materials mainly follows First order model or Higuchi one [54][55][56][57]. While the First Order model is general, the Higuchi one can be used for the description of drug release from spherical systems and various geometric porous matrices [58].…”
Section: Kinetics Of Drug Releasementioning
confidence: 99%
“…Among the developed nano-carriers, mesoporous silica nanoparticles (MSN) [17][18][19][20][21][22][23][24][25][26][27][28] have shown great potential for applications in drug delivery vehicles due to its biocompatibility, high surface area, and tendency to undergo cellular uptake into acidic lysosomes by endocytosis when having a diameter of 100-200 nm. Consequently, several drug delivery systems based on MSNs have been developed during the last decade [29][30][31][32][33][34][35][36][37][38][39][40][41][42]. In these systems, controlled release of drug can be achieved in response to various stimuli such as light, redox potential, temperature, pH and enzymes.…”
Section: Introductionmentioning
confidence: 99%
“…Various pH responsive MSN have been developed using different capping agents, such as polymer, biomolecules and also inorganic nanoparticles [37,38,[43][44][45][46][47][48][49][50] The challenge here is to find the responsive capping agent that can effectively release the drug selectively on the cancer cells.…”
Section: Introductionmentioning
confidence: 99%