A pH-sensitive silica nanoparticles for colon-specific delivery and controlled release of catechin: Optimization of loading efficiency and in vitro release kinetics

被引:13
|
作者
Kassem, Abdulsalam M. [1 ]
Almukainzi, May [2 ]
Faris, Tarek M. [2 ]
Ibrahim, Ahmed H. [1 ]
Anwar, Walid [1 ]
Elbahwy, Ibrahim A. [1 ]
El-Gamal, Farid R. [1 ]
Zidan, Mohamed F. [1 ]
Akl, Mohamed A. [1 ,3 ]
Abd-ElGawad, Ahmed M. [4 ]
Elshamy, Abdelsamed I. [5 ]
Elmowafy, Mohammed [1 ,6 ]
机构
[1] Al Azhar Univ, Fac Pharm Boys, Dept Pharmaceut & Pharmaceut Technol, Cairo 11751, Egypt
[2] Princess Nourah Bint Abdulrahman Univ, Coll Pharm, Dept Pharmaceut Sci, POB 84428, Riyadh 11671, Saudi Arabia
[3] Islamic Univ, Coll Pharm, Dept Pharmaceut, Najaf 54001, Iraq
[4] Mansoura Univ, Fac Sci, Dept Bot, Mansoura 35516, Egypt
[5] Natl Res Ctr, Chem Nat Cpds Dept, 33 El Bohouth St, Dokki 12622, Giza, Egypt
[6] Jouf Univ, Coll Pharm, Dept Pharmaceut, POB 2014, Sakaka, Saudi Arabia
关键词
Mesoporous silica nanoparticles; Catechin; pH-responsive drug delivery system; Colon targeting; Eudragit (R)-S100; CONTROLLED DRUG-DELIVERY; MESOPOROUS SILICA; CHITOSAN NANOPARTICLES; SUSTAINED-RELEASE; ANTIOXIDANT; POLYMER; CYCLODEXTRIN; QUERCETIN; MICROPARTICLES; POLYPHENOLS;
D O I
10.1016/j.ejps.2023.106652
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Catechin is a naturally occurring flavonoid of the flavan-3-ol subclass with numerous biological functions; however, these benefits are diminished due to several factors, including low water solubility and degradation in the stomach's harsh environment. So, this study aimed to develop an intelligent catechin colon-targeting delivery system with a high loading capacity. This was done by coating surface-decorated mesoporous silica nanoparticles with a pH-responsive enteric polymer called Eudragit (R)-S100. The pristine wormlike mesoporous silica nanoparticles (< 100 nm) with high surface area and large total pore volume were effectively synthesized and modified with the NH(2 )group using the post-grafting strategy. Various parameters, including solvent polarity, catechin-carrier mass ratio, and adsorption time, were studied to improve the loading of catechin into the aminated silica nanoparticles. Next, the negatively charged Eudragit (R)-S100 was electrostatically coated onto the positively charged aminated nanocarriers to shield the loaded catechin from the acidic environment of the stomach (pH 1.9) and to facilitate site-specific delivery in the acidic environment of the colon (pH 7.4). The prepared nanomaterials were evaluated using several methods, including The Brauner-Emmett-Teller, surface area analyzer, zeta sizer, Field Emission Scanning Electron Microscope, Powder X-Ray Diffraction, Fourier Transform Infrared Spectroscopy, Energy-Dispersive X-ray Spectroscopy, and Differential Scanning Calorimetry. In vitro dissolution studies revealed that Eudragit (R)-S100-coated aminated nanomaterials prevented the burst release of the loaded catechin in the acidic environment, with approximately 90% of the catechin only being released at colonic pH (pH > 7) with a supercase II transport mechanism. As a result, silica nanoparticles coated with Eudragit (R)-S100 would provide an innovative and promising approach in targeted nanomedicine for the oral delivery of catechin and related medicines for treating diseases related to the colon, such as colorectal cancer and irritable bowel syndrome.
引用
收藏
页数:17
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