Mesoporous silica nanoparticles as vehicles for drug delivery

Adristya, I Made, Suryaningtyas, Ayu Dhea, Wijaya, Jenifer, Pangestu, Felisia Cahyani, Hartono, Sandy Budi, Hadisoewignyo, Lannie and Irawaty, Wenny (2020) Mesoporous silica nanoparticles as vehicles for drug delivery. IOP Conference Series: Materials Science and Engineering, 778. pp. 1-6. ISSN 1757-899X

[thumbnail of Mesoporous silica nanoparticles as vehicles for drug delivery] Text (Mesoporous silica nanoparticles as vehicles for drug delivery)
Rev Mesoporous_Artikel Repository.pdf
Restricted to Registered users only

Download (3MB) | Request a copy
[thumbnail of Mesoporous silica nanoparticles as vehicles for drug delivery_peer_review_] Text (Mesoporous silica nanoparticles as vehicles for drug delivery_peer_review_)
Rev Mesoporous_silica_Peer Review.pdf
Restricted to Registered users only

Download (1MB) | Request a copy
[thumbnail of Mesoporous silica nanoparticles as vehicles for drug delivery] Text (Mesoporous silica nanoparticles as vehicles for drug delivery)
Mesoporous_silica_NP_Hasil Cek Similarity.pdf
Restricted to Registered users only

Download (1MB) | Request a copy

Abstract

Silica-based materials such as mesoporous silica nanoparticle MCM-41 and hollow mesoporous silica have been synthesized at room temperature. Several characterization techniques such as N2 adsorption-desorption analysis, SEM and FTIR have been employed to assess the formation of the nanoparticles. Rifampicin, commonly used in tuberculosis treatment, was selected as the target drug to assess the ability of the two nanoparticles to host this antibiotic. Following the loading of rifampicin on the particle surface, the dissolution behaviour of rifampicin in a media was investigated. Surface characterizations show HMS exhibits higher surface area as well as pore size and volume compared to MCM-41. However, rifampicin was not attached on the latter particles until it was modified with APTES. HMS particles store more rifampicin molecules on the particle surface than the modified MCM-41. The in-vitro drug release was investigated with buffer phosphate (pH=7.4) and the results shown that the rifampicin-loaded HMS particles were capable of releasing 18% rifampicin content after 77 h. Further investigation was necessary to support the promising application of mesoporous silica nanoparticles for pulmonary drug delivery.

Item Type: Article
Uncontrolled Keywords: silica nanoparticles, mesoporous, drug delivery, rifampicin
Subjects: Engineering > Chemical Engineering
Divisions: Faculty of Engineering > Chemical Engineering Study Program
Depositing User: Wenny Irawaty
Date Deposited: 28 Aug 2020 04:45
Last Modified: 02 Apr 2022 05:46
URI: https://repository.ukwms.ac.id/id/eprint/21894

Actions (login required)

View Item View Item