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合成羧酸 - 二醛纤维素以用作伤口敷料抗菌材料复合薄膜的一种成分。

Synthesis of Carboxylate-Dialdehyde Cellulose to Use as a Component in Composite Thin Films for an Antibacterial Material in Wound Dressing.

作者信息

Chaiwarit Tanpong, Duangsonk Kwanjit, Yuantrakul Sastra, Chanabodeechalermrung Baramee, Khangtragool Waristha, Brachais Claire-Hélène, Chambin Odile, Jantrawut Pensak

机构信息

Department of Pharmaceutical Sciences, Faculty of Pharmacy, Chiang Mai University, Chiang Mai 50200, Thailand.

Department of Microbiology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.

出版信息

ACS Omega. 2024 Oct 24;9(44):44825-44836. doi: 10.1021/acsomega.4c08298. eCollection 2024 Nov 5.

Abstract

Wound infections can lead to life-threatening infection and death. Antibacterial materials from biopolymers in the form of films are a promising strategy for wound dressings. Carboxylate-dialdehyde cellulose (CDAC) is a proper candidate for use as an antibacterial material due to its biocompatibility, nontoxicity, and antibacterial property. Additionally, CDAC can be synthesized from cellulose through environmentally friendly and nontoxic methods. Thus, this study aims to synthesize CDAC from microcrystalline cellulose (MCC) PH102 and use it in composite films for an antibacterial application. The CDAC was synthesized using Fe/HO, followed by NaIO oxidation. The obtained CDAC was characterized in terms of carboxylate and aldehyde content as well as FTIR and XRD spectra. The CDAC was mixed with HPMC in different ratios to prepare films. To determine the optimal formulation for clindamycin HCl loading, the films were evaluated for morphology, mechanical properties, and swelling ratio. Finally, the films containing clindamycin HCl were evaluated for drug loading content, drug release, and antibacterial activity. This study found that CDAC contained 2.1 ± 0.2 carboxylate and 4.15 ± 0.2 mmol/g of aldehyde content. The FTIR spectra confirmed the successful synthesis. X-ray diffractograms indicated that CDAC was less crystalline than MCC. The film, consisting of CDAC and HPMC E50 in the ratio of 2:1 (D2H1), was identified as the most suitable for clindamycin HCl loading due to its superior appearance, mechanical strength, and swelling properties compared to other formulations. D2H1 exhibited a high drug loading capacity (91.49 ± 5.48%) and demonstrated faster drug release than the film composed only of HPMC because of the higher swelling ratio and lower mechanical strength. This formulation was effective against (MSSA), (MRSA), and . Furthermore, the D2H1 film containing clindamycin HCl showed a larger inhibition zone against these bacteria, likely due to a synergistic effect. This study found that CDAC has the potential to be applied as an antibacterial material for wound dressing.

摘要

伤口感染可导致危及生命的感染甚至死亡。以薄膜形式存在的生物聚合物抗菌材料是伤口敷料的一种有前景的策略。羧基二醛纤维素(CDAC)因其生物相容性、无毒性和抗菌性能,是用作抗菌材料的合适候选物。此外,CDAC可通过环境友好且无毒的方法由纤维素合成。因此,本研究旨在从微晶纤维素(MCC)PH102合成CDAC,并将其用于复合薄膜的抗菌应用。使用Fe/HO合成CDAC,随后进行NaIO氧化。对所得的CDAC进行羧基和醛含量以及傅里叶变换红外光谱(FTIR)和X射线衍射(XRD)光谱表征。将CDAC与羟丙基甲基纤维素(HPMC)按不同比例混合以制备薄膜。为确定盐酸克林霉素负载的最佳配方,对薄膜的形态、机械性能和溶胀率进行评估。最后,对含盐酸克林霉素的薄膜进行载药量、药物释放和抗菌活性评估。本研究发现CDAC含有2.1±0.2个羧基和4.15±0.2 mmol/g的醛含量。FTIR光谱证实合成成功。X射线衍射图表明CDAC的结晶度低于MCC。由CDAC和HPMC E50按2:1比例组成(D₂H₁)的薄膜,因其外观、机械强度和溶胀性能优于其他配方,被确定为最适合盐酸克林霉素负载。D₂H₁表现出高载药量(91.49±5.48%),并且由于较高的溶胀率和较低的机械强度,其药物释放速度比仅由HPMC组成的薄膜更快。该配方对甲氧西林敏感金黄色葡萄球菌(MSSA)、耐甲氧西林金黄色葡萄球菌(MRSA)和[此处原文缺失一种细菌名称]有效。此外,含盐酸克林霉素的D₂H₁薄膜对这些细菌显示出更大的抑菌圈,这可能是由于协同作用。本研究发现CDAC有潜力用作伤口敷料的抗菌材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e32/11541528/6c86914c852e/ao4c08298_0002.jpg

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