## Abstract The amino terminus truncated p73 isoform, ΔNp73α, shows dominant negative behavior toward TAp73 and wild‐type p53, and has oncogenic potential. By contrast, we recently showed that in HCT116 clones forced expression of ΔNp73α did not increase __in vitro__ cellular resistance to anticanc
In vivo evaluation of injectable thermosensitive polymer with time-dependent LCST
✍ Scribed by Eric Henderson; Bae Hoon Lee; Zhanwu Cui; Ryan McLemore; Tedd A. Brandon; Brent L. Vernon
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 703 KB
- Volume
- 90A
- Category
- Article
- ISSN
- 1549-3296
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The focus of this study was to examine the biocompatibility, time‐dependent LCST, and bioerodable properties of a copolymer system composed of NIPAAm, dimethyl‐γ‐butyrolactone (DMBL), and acrylic acid (AAc). Sprague Dawley rats were subcutaneously injected with 25 wt % solutions of poly(NIPAAm‐co‐DMBL‐co‐AAc). At predetermined times, animals were sacrificed and polymer implants were recovered for characterization via ^1^H‐NMR. In addition, polymer‐contacting tissue sections were harvested and processed for histology. The biocompatibility of the implants was assessed by counting the number of fibroblasts and leukocytes present at the tissue‐implant interface. The LCST data obtained from the in vivo implants was shown to agree with that of in vitro findings. Implant mass was shown to decrease after 4 days, indicating accelerated diffusion rates with increased implant swelling, hydrolytic degradation was confirmed with ^1^H‐NMR measurements. The cellular presence at the copolymer implant‐tissue interface was shown to return to that of normal tissue 30 days postimplantation, which suggests a normal wound healing response. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res, 2009
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