2014
DOI: 10.1016/j.saa.2013.09.132
|View full text |Cite
|
Sign up to set email alerts
|

Modification of chitosan by using samarium for potential use in drug delivery system

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

2
13
0
5

Year Published

2014
2014
2020
2020

Publication Types

Select...
7
2

Relationship

3
6

Authors

Journals

citations
Cited by 18 publications
(20 citation statements)
references
References 16 publications
2
13
0
5
Order By: Relevance
“…The narrow distribution indicates that the chitosan nanoparticles produced would be suitable as drug carriers for delivery. Drug carriers characterized by homogeneous and small particle sizes and similar morphology are more efficient for drug loading and delivery (Yang et al, 2010;Kusrini et al, 2014).…”
Section: Particle Size Distribution Studiesmentioning
confidence: 99%
“…The narrow distribution indicates that the chitosan nanoparticles produced would be suitable as drug carriers for delivery. Drug carriers characterized by homogeneous and small particle sizes and similar morphology are more efficient for drug loading and delivery (Yang et al, 2010;Kusrini et al, 2014).…”
Section: Particle Size Distribution Studiesmentioning
confidence: 99%
“…Fluorescence intensity of microsphere formulations increased with the cumulative 030011-3 amount release of ranitidine, so that the changing of fluorescence intensity at wavelength of 590 nm referring to the Sm 3+ ion could be used as indicator in DDS. The Sm 3+ ions was bonded with the hydroxyl groups of chitosan that resulted Sm 3+ ions fluorescence intensity increases with the ranitidine cumulative amount released from the Chit/Sm/Fe3O4/Rn [5]. The existence of samarium in the chitosan matrix has function as a tracer or marker of drug release.…”
Section: Figure 1 (A) Xrd Characterization Results Of Fe3o4 (B) Vsm mentioning
confidence: 99%
“…Preparation of drug adsorption and release system were prepared in accordance with literature [5]. In drug loading, 50 mg matrices was dissolved in 25 ml of distilled water and then allowed to stand for 24 h. After 24 h, retentate and the filtrate was measured its absorbance by using UV-Vis spectrophotometry.…”
Section: Drug Loading and Drug Release Studiesmentioning
confidence: 99%
“…Luo et al has discussed about Nano/micro particle, hydrogel beads, layer by layer film based chitosan DDS system [9]. Kusrini et al has modified chitosan using samarium to improve drug release [10]. Bernkop-Schnrch et al has discussed about the cationic nature of chitosan for controlled drug delivery applications.…”
Section: Introductionmentioning
confidence: 99%