Experimental Study of Drug Delivery system for Prednisolone Loaded and Released by Mesoporous Silica MCM-41

Keywords

Drug delivery, Kinetics model, MCM-41, Prednisolone.

How to Cite

Experimental Study of Drug Delivery system for Prednisolone Loaded and Released by Mesoporous Silica MCM-41. (2019). Al-Khwarizmi Engineering Journal, 15(1), 117-124. https://doi.org/10.22153/kej.2019.06.004

Abstract

In the present study, nanoporous material type MCM-41 was prepared by the sol-gel technique and was used as a carrier for prednisolone (PRD) drug delivery. The structural properties of mesoporous were fully characterized by X-ray diffraction (XRD), N2 adsorption /desorption and Fourier-transform infrared (FTIR). The mass transfer in term of adsorption process (loading) and desorption process (releasing) properties were investigated. The maximum drug loading efficiency was equal to 38% and 47.5% at different concentrations. The PRD released was prudently studied in water media of pH 6.8 simulated body fluid (SBF) in according to "United State Pharmacopeia (USP38)". The results proved that the release of prednisolone from MCM-41 was (69.4%) after 24 hr. The data of the released PRD was found to be submitted to a Korsmeyer–Peppas model.

References

Pang, J., Luan, Y., Li, F., Cai, X., & Li, Z. (2010). Ionic liquid-assisted synthesis of silica particles and their application in drug release. Materials letters, 64(22), 2509-2512.‏

Burness, L. T. (2009). Mesoporous materials: properties, preparation, and applications. Nova Science Publishers.‏

Popova, M., Trendafilova, I., Szegedi, Á., Mihály, J., Németh, P., Marinova, S. G., & Vayssilov, G. N. (2016). Experimental and theoretical study of quercetin complexes formed on pure silica and Zn-modified mesoporous MCM-41 and SBA-16 materials. Microporous and Mesoporous Materials, 228, 256-265.

Yilmaz, M. S., Palantoken, A., & Piskin, S. (2016). Release of flurbiprofen using of SBA-15 mesoporous silica: influence of silica sources and functionalization. Journal of Non-Crystalline Solids, 437, 80-86.‏

Popat, A., Hartono, S. B., Stahr, F., Liu, J., Qiao, S. Z., & Lu, G. Q. M. (2011). Mesoporous silica nanoparticles for bioadsorption, enzyme immobilisation, and delivery carriers. Nanoscale, 3(7), 2801-2818.

Vallet-Regi, M., Ramila, A., Del Real, R. P., & Pérez-Pariente, J. (2001). A new property of MCM-41: drug delivery system. Chemistry of Materials, 13(2), 308-311.‏

Tsybko, A. S., Amstislavskaya, T. G., Kontsevaya, G. V., & Gerlinskaya, L. A. (2014). Effect of chronic inhalation of silicon dioxide nanoparticles (Tarkosil 25) on the expression of key genes of the serotonergic system in the mouse brain. Nanotechnologies in Russia, 9(3-4), 213-218.‏

Lay, C. L., Liu, H. Q., Wu, D., & Liu, Y. (2010). Poly (ethylene glycol) ‐Graft‐Hollow Silica Vesicles for Drug Delivery. Chemistry-A European Journal, 16(10), 3001-3004.

Shen, S. C., Ng, W. K., Chia, L., Hu, J., ..& Tan, R. B. (2011). Physical state and dissolution of ibuprofen formulated by co-spray drying with mesoporous silica: effect of pore and particle size. International journal of pharmaceutics, 410(1-2), 188-195.

Chen, Z., Li, X., He, H., Ren, Z., Liu, Y., Wang, J., ... & Han, G. (2012). Mesoporous silica nanoparticles with manipulated microstructures for drug delivery. Colloids and Surfaces B: Biointerfaces, 95, 274-278.‏

Tsai, C. P., Hung, Y., Chou, Y. H., Huang, D. M., Hsiao, J. K., Chang, C., ... & Mou, C. Y. (2008). High‐Contrast Paramagnetic Fluorescent Mesoporous Silica Nanorods as a Multifunctional Cell‐Imaging Probe. Small, 4(2), 186-191.‏

Cavallaro, G., Pierro, P., Palumbo, F. S., Testa, F., Pasqua, L., & Aiello, R. (2004). Drug delivery devices based on mesoporous silicate. Drug Delivery, 11(1), 41-46.‏

Qu, F., Zhu, G., Huang, S., Li, S., & Qiu, S. (2006). Effective Controlled Release of Captopril by Silylation of Mesoporous MCM‐41. Chem Phys Chem, 7(2), 400- 406.‏

Porter, R.S., 2011. The Merck Manual of Diagnosis and Therapy. Wiley.

Ashok, R., Prakash, P. P., & Tamil Selvan, R. (2011). Development and validation of analytical method for estimation of prednisolone in bulk and tablets using UV-Visible spectroscopy. Int J Pharm Pharm Sci, 3(4), 184-6.

Albayati, T. M., Alwan, G. M., & Mahdy, O. S. (2017). High performance methyl orange capture on magnetic nanoporous MCM-41 prepared by incipient wetness impregnation

method. Korean Journal of Chemical Engineering, 34(1), 259-265.‏

Ahmadi, E., Dehghannejad, N., Hashemikia, S., Ghasemnejad, M., & Tabebordbar, H. (2014). Synthesis and surface modification of mesoporous silica nanoparticles and its application as carriers for sustained drug delivery. Drug delivery, 21(3), 164-172.‏

Ayad, M. M., Salahuddin, N. A., El-Nasr, A. A., & Torad, N. L. (2016). Amine-functionalized mesoporous silica KIT-6 as a controlled release drug delivery carrier. Microporous and Mesoporous Materials, 229, 166-177.‏

Chen, X. Y., Shang, Y. L., Li, Y. H., Wang, J. X., Maimouna, A. G., Li, Y. X., & Pu, Y. (2015). Green preparation of uniform prednisolone nanoparticles using subcritical water. Chemical Engineering Journal, 263, 20-26.‏

Costa, J. A., Garcia, A. C., Santos, D. O., Sarmento, V. H., Porto, A. L., Mesquita, M. E. D., & Romão, L. P. (2014). A new functionalized MCM-41 mesoporous material for use in environmental applications. Journal of the Brazilian Chemical Society, 25(2), 197-207.‏

Farjadian, F., Ahmadpour, P., Samani, S. M., & Hosseini, M. (2015). Controlled size synthesis and application of nanosphere MCM-41 as potent adsorber of drugs: a novel approach to new antidote agent for intoxication. Microporous and Mesoporous Materials, 213, 30-39.

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