2014
DOI: 10.1007/s10570-014-0515-9
|View full text |Cite
|
Sign up to set email alerts
|

Cellulose based thin films as a platform for drug release studies to mimick wound dressing materials

Abstract: In this paper, the use of ultrathin cellulose supports as platform for the incorporation of analgesic drugs in wound dressings is proposed. As a model drug, diclofenac (DCF) is chosen, which is commonly used in pain easing medical treatments. The DCF containing cellulose films are prepared by mixing solutions of trimethylsilyl cellulose (DS Si :2.5) with DCF dissolved in THF. After depositing the material on a solid surface by spin-coating, the films are subjected to vapor-phase hydrolysis using 3 M HCl in ord… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
39
0

Year Published

2015
2015
2023
2023

Publication Types

Select...
5
2

Relationship

2
5

Authors

Journals

citations
Cited by 58 publications
(39 citation statements)
references
References 32 publications
0
39
0
Order By: Relevance
“…[30][31][32] Mostly NSAIDs are taken through systemic administration (i.e., in the form of pills), whereas several approaches have been and are researched towards their integration into different wound dressing formulations. [33][34][35][36] Although antibiotics are not the preferred type of drugs for local treatment due to possible resistance acquisition of commensal bacteria, there are several interesting studies available about preparation of dressing, combining NSAIDs and antimicrobials. [37][38][39] The purpose of this study was therefore to prepare wound dressing materials with incorporated NSAIDs and to study their efficiency related to material performance and drug release.…”
Section: Introductionmentioning
confidence: 99%
“…[30][31][32] Mostly NSAIDs are taken through systemic administration (i.e., in the form of pills), whereas several approaches have been and are researched towards their integration into different wound dressing formulations. [33][34][35][36] Although antibiotics are not the preferred type of drugs for local treatment due to possible resistance acquisition of commensal bacteria, there are several interesting studies available about preparation of dressing, combining NSAIDs and antimicrobials. [37][38][39] The purpose of this study was therefore to prepare wound dressing materials with incorporated NSAIDs and to study their efficiency related to material performance and drug release.…”
Section: Introductionmentioning
confidence: 99%
“…At 1577 cm −1 , R=C=O stretching vibration is observed. Additional peaks corresponding to R–C=O stretching and CH 2 bending are visible at 1305 and 1462 cm −1  6172. Although small in intensity, these peaks are visible for all samples with DCF as the top layer.…”
Section: Resultsmentioning
confidence: 90%
“…For this purpose, we applied several models to describe the respective release profiles according to909192. The authors of the present study have studied different materials and their release performances before589394959697. Unfortunately, as simple as our system may seem (schematically depicted in Fig.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The core layer is made of fabric, which releases drug differentially at different pH values, with maximum release of drug in acidic medium. To decelerate the release rate, Maver et al proposed ultrathin cellulose supports as a platform for the incorporation of analgesic drugs in wound dressings. This dressing sustained the release of the entrapped drug and maintained the antibacterial activity up to 12 days .…”
Section: Discussionmentioning
confidence: 99%