journal article·2017-01-26Open access

Macro-Scale Model Study of a Tunable Drug Dispensation Mechanism for Controlled Drug Delivery in Potential Wound-Healing Applications

Mariam Mir, Umar Ansari, Murtaza Najabat Ali

Abstract

Background Auxetic materials tend to exhibit stretching in the direction of the applied load as well as in the perpendicular direction. This may be an inherent property of the material, or it might be a particular structural characteristic that confers it with auxetic properties. In this study, the auxetic properties of a rotating squares auxetic design were utilized in tandem with a stretching mechanism to manufacture a device that offers the advantages of adjustable pore size and hence tunable drug delivery characteristics. Methods An auxetic polyurethane film was fabricated through the polymer casting technique. An acrylonitrile-butadiene-styrene (ABS) plastic mold for polymer casting was made through additive manufacturing. Stereolithography was used for fabrication of the mechanism that controlled pore size of the polymeric auxetic film. A laminate arrangement of the film and the mechanism was devised, through which movement of the mechanism controlled stretching of the auxetic film underneath. Results Results were analyzed through image processing. It was observed that a 2-dimensional increase (in length and width) of the auxetic film took place that corresponded to an increase in pore size of the film. Several mathematical correlations were drawn up. Conclusions It may be concluded that the first factor controlling drug release kinetics is the pore size of the film. This study explored a prototype mechanism that has the potential for being used in devices for controlled drug delivery or in smart bandage systems that may enhance wound healing in chronic wound treatment.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Cellular and Composite Structures · Polymer Foaming and Composites · Bone Tissue Engineering Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Biomedical Engineering and Sciences Department, School of Mechanical and Manufacturing Engineering, National University of Sciences and Technology (NUST), Islamabad - Pakistan

References (21)

Show source-provided references
1. 10.1016/0738-081X(94)90262-310.1016/0738-081X(94)90262-3 ↗
2. 10.1002/bjs.180067120510.1002/bjs.1800671205 ↗
3. 10.1177/002203450935912510.1177/0022034509359125 ↗
4. 10.1163/15685620777999691310.1163/156856207779996913 ↗
5. HuangX BrazelCS On the importance and mechanisms of burst release in matrix-controlled drug delivery systems. 2001732-3121–136
6. AndersonJM KimSWeds. Recent advances in drug delivery systems. Boston, MA Springer 198410.1007/978-1-4613-2745-5 ↗
7. 10.1016/S0168-3659(99)00194-710.1016/S0168-3659(99)00194-7 ↗
8. 10.12968/jowc.2011.20.7.31910.12968/jowc.2011.20.7.319 ↗
9. Polymers in controlled drug delivery. MDDI Medical Device and Diagnostic Industry News Products and Suppliers 1997
10. 10.4155/tde.10.1610.4155/tde.10.16 ↗
11. UjangZ1 Abdul RashidAH SubohSK HalimAS LimCK Physical properties and biocompatibility of oligochitosan membrane film as wound dressing, J Appl Biomater Funct Mater. 2014 30123155–162
12. 10.1080/0098644800891251910.1080/00986448008912519 ↗
13. 10.1016/0378-5173(88)90245-110.1016/0378-5173(88)90245-1 ↗
14. 10.1016/S1359-6454(99)00299-210.1016/S1359-6454(99)00299-2 ↗
15. 10.1557/PROC-331-21110.1557/PROC-331-211 ↗
16. 10.1016/j.ijpharm.2008.07.03310.1016/j.ijpharm.2008.07.033 ↗
17. 10.1016/j.jconrel.2007.08.01710.1016/j.jconrel.2007.08.017 ↗
18. 10.1088/0022-3727/22/12/01210.1088/0022-3727/22/12/012 ↗
19. 10.1038/353124a010.1038/353124a0 ↗
20. 10.1080/0892702050038585210.1080/08927020500385852 ↗
21. 10.1002/pssb.20098203510.1002/pssb.200982035 ↗