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Mechanism study on pH-responsive cyclodextrin capped mesoporous silica: effect of different stalk densities and the type of cyclodextrin
被引:26
|作者:
Bai, Ling
[1
]
Zhao, Qinfu
[1
]
Wang, Jian
[3
]
Gao, Yikun
[2
]
Sha, Zhou
[1
]
Di, Donghua
[1
]
Han, Ning
[1
]
Wang, Ying
[1
]
Zhang, Jinghai
[2
]
Wang, Siling
[1
]
机构:
[1] Shenyang Pharmaceut Univ, Liaoning Prov Key Lab Studying Modern Drug Prepar, 103 Wenhua Rd, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Med Devices, Shenyang 110016, Peoples R China
[3] Shenyang Pharmaceut Univ, Minist Educ, Key Lab Struct Based Drug Design & Discovery, Shenyang 110016, Peoples R China
基金:
中国国家自然科学基金;
关键词:
mesoporous silica nanoparticles;
pH-responsive;
stalk density;
cyclodextrin;
controlled release system;
CONTROLLED-RELEASE;
DRUG-DELIVERY;
BETA-CYCLODEXTRIN;
GUEST MOLECULES;
NANOPARTICLES;
BIOCOMPATIBILITY;
COMPLEXATION;
NAPROXEN;
STIMULI;
THERAPY;
D O I:
10.1088/0957-4484/26/16/165704
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Cyclodextrin (CD)-capped mesoporous silica nanoparticles (MSN) with pH-responsive properties were synthesized, but little research has been carried out to evaluate the impact of critical factors such as the stalk density and the type of CD on the pH-responsive release behavior. Here, the effect of different stalk densities on the pH-responsive release behavior was investigated. Either too low or too high density of the grafted p-anisidine stalk could result in poor cargo release, and the optimum stalk density for MSN was measured by thermal analysis, and found to be approximately 8.7 stalks nm(-2). To achieve effective release control, the CD capes, alpha-CD and beta-CD, were also investigated. Isothermal titration calorimetry (ITC) analysis was employed to determine the formation constants (K-f) of the two CD with p-anisidine at different pH values. The results obtained showed that the complex of beta-CD with p-anisidine had excellent pH-responsive behavior as it exhibited the largest changed formation constant (Delta K-f) in different pH media. Furthermore, the pH-responsive mechanism between CD and p-anisidine molecules was investigated through ITC and a molecular modeling study. The release of antitumor drug DOX presents a significant prospect toward the development of pH-responsive nanoparticles as a drug delivery vehicle.
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页数:11
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