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1.大理大学云南省昆虫生物医药研发重点实验室,云南 大理 671000
2.大理大学药用特种昆虫开发国家地方联合工程研究中心,云南 大理 671000
3.大理大学中国西南药用昆虫及蛛形类资源开发利用协同创新中心,云南 大理 671000
4.南京中医药大学药学院,南京 210023
5.云南省第一人民医院牙周科,昆明 650032
硕士研究生。研究方向:昆虫生物医药。E-mail:zhn970611@163.com
教授,博士生导师,博士。研究方向:天然药物及生物资源研究与开发。E-mail:dryuzhao@126.com
纸质出版日期:2023-01-30,
收稿日期:2022-06-21,
修回日期:2022-08-15,
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曾惠娜,卿晨,薛楠楠等.载美洲大蠊提取物蛛丝蛋白膜的制备、表征及体外释药性和细胞毒性考察 Δ[J].中国药房,2023,34(02):168-172.
ZENG Huina,QING Chen,XUE Nannan,et al.Preparation, characterization, in vitro drug release property and cytotoxicity of Periplaneta americana extract-loaded spider fibroin membrane[J].ZHONGGUO YAOFANG,2023,34(02):168-172.
曾惠娜,卿晨,薛楠楠等.载美洲大蠊提取物蛛丝蛋白膜的制备、表征及体外释药性和细胞毒性考察 Δ[J].中国药房,2023,34(02):168-172. DOI: 10.6039/j.issn.1001-0408.2023.02.08.
ZENG Huina,QING Chen,XUE Nannan,et al.Preparation, characterization, in vitro drug release property and cytotoxicity of Periplaneta americana extract-loaded spider fibroin membrane[J].ZHONGGUO YAOFANG,2023,34(02):168-172. DOI: 10.6039/j.issn.1001-0408.2023.02.08.
目的
2
制备一种载美洲大蠊提取物的蛛丝蛋白膜,并对其进行表征及体外释药性和细胞毒性考察。
方法
2
以天然敬钊缨毛蛛蛛丝为原料,美洲大蠊提取物为模型药物,采用溶剂浇铸法制备载药蛛丝蛋白膜(后文称“载药膜”),同法制备不含美洲大蠊提取物的载药材料基质蛛丝蛋白膜(后文称“空白膜”)。经静态水接触角、傅里叶红外色谱、X-射线衍射以及扫描电镜等技术对膜剂进行表征,从不同角度分析膜剂结构;通过体外模拟药物在人工唾液中的释放特性评价药物的缓释性能;以MTT法验证载药膜的体外细胞毒性。
结果
2
制备得到的载药膜的静态水接触角均小于90°,且小于空白膜;载药膜在1 500~1 700 cm
-1
存在美洲大蠊提取物多肽的特征吸收峰;同时X-射线衍射和扫描电镜也证实美洲大蠊提取物已成功负载到膜剂中。该膜剂可在人工唾液中释药时长逾200 min。MTT实验结果显示,空白膜和载药膜作用后的细胞增殖率分别为84.6%、79.4%(均大于70%),无显著的潜在细胞毒性。
结论
2
以天然蛛丝所制备的载药膜在人工唾液中具有一定的缓释效果,有望作为一种具优异生物相容性的药物缓释载体应用于临床。
OBJECTIVE
2
To prepare spider fibroin membrane loaded with
Periplaneta americana
extract, and investigate its characterization,
in vitro
drug release property and cytotoxicity.
METHODS
2
Using natural
spider silk collected from
Chilobrachys guangxiensis
as raw material,
P. americana
extract as model drug, the drug-loaded spider fibroin membrane (hereinafter referred to as drug-loaded membrane) was prepared by solvent casting method. The material matrix spider fibroin membrane without
P. americana
extract (hereinafter referred to as blank membrane) was prepared with same method. The membrane structure was characterized by static water contact angle, Fourier infrared chromatography, X-ray diffraction and scanning electron microscopy from different angles; drug release characteristics in artificial saliva were simulated
in vitro
to evaluate the drug sustained-release performance. MTT assay was adopted to validate the cytotoxicity of drug-loaded membrane.
RESULTS
2
The drug-loaded membrane was prepared, and the static water contact angle was less than 90°, which was less than that of blank membrane.
The drug-loaded membrane showed the characteristic absorption peak to polypeptide of
P. americana
extract at 1 500-1 700 cm
-1
.
X-ray diffraction and scanning electron microscopy also proved that the drug was successfully loaded into the pellicle. The release time of the pellicle in artificial saliva was more than 200 min. The MTT test results showed that the cell proliferation rates of blank membrane and drug-loaded membrane were 84.6% and 79.4% (both greater than 70%), respectively, without significant potential cytotoxicity.
CONCLUSIONS
2
Drug-loaded membrane prepared with natural
spider silk has a certain sustained-release effect in artificial saliva, which can be further developed as a drug sustained-release carrier with excellent biological characteristics and biocompatibility.
美洲大蠊口腔膜剂天然蛛丝敬钊缨毛蛛蛛丝蛋白膜药物缓释含量测定细胞毒性
oral pelliclesnatural spider silkChilobrachys guangxiensisspider fibroin membranedrug sustained-releasecontent determinationcytotoxicity
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