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首页> 外文期刊>Journal of nanoscience and nanotechnology >Preparation of Ethosomes and Deformable Liposomes Encapsulated with 5-Fluorouracil and Their Investigation of Permeability and Retention in Hypertrophic Scar
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Preparation of Ethosomes and Deformable Liposomes Encapsulated with 5-Fluorouracil and Their Investigation of Permeability and Retention in Hypertrophic Scar

机译:5-氟尿嘧啶包裹的脂质体和可变形脂质体的制备及其在肥厚性瘢痕中的通透性和滞留性的研究

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With the aim of comparing scar penetration efficiency and retention between ethosomes and deformable liposomes both encapsulated with 5-fluorouracil (5-FU), the 5-FU ethosomal suspensions (5-FU ES, 81.74 ± 9.37 nm) and the 5-FU Deformable Liposomal Suspensions (5-FU DS, 73.7 ± 9.45 nm) were prepared respectively by Touitou method and Cevc method, their sizes were determined by Particle Sizer System (PSS), and their entrapment Efficiency (EE) was detected by ultracentrifugation and microcolumn centrifugation. Their transdermal delivery experiments were done in hypertrophic scars in vitro. The permeated amount of 5-FU and retention contents of 5-FU were both calculated by High Performance Liquid Chromatography (HPLC). Fluorescence intensities of ES and DS labeled with Rodanmin 6GO (Rho) were measured by Laser Scanning Microscopy (LSM). The control groups such as the 5-FU and empty ethosomal vesicles (5-FU + EEV), the 5-FU and empty deformable liposomal vesicles (5-FU + EDV) and 5-FU PBS Solution (5-FU Sol) were set up. Results showed that, prepared 5-FU ES was 81.74 ± 9.37 nm in size, 5-FU DS was 73.7±9.45 nm, EE of 5-FU ES was 10.95%, EE of 5-FU DS was 15.05%. Within 24 hours, in the group of 5-FU ES, the penetration amount of 5-FU in scar was 14.12 ± 0.1 μg/mL/cm~2, the retention contents of 5-FU was 10.74±1.17 μg/cm~2, and the fluorescence intensity of Rho in hyper-trophic scar tissues were 182 ± 18.3; in the group of 5-FU DS: the penetration amount of 5-FU was 12.35±1.21 μg/mL/cm~2; the retention contents of 5-FU was 17.48 ± 0.82 μg/cm~2, and the fluorescence intensity of Rho was 241.45 ± 7.63; there existed statistical difference between penetration amount in the group of 5-FU ES and that in the group of 5-FU DS as well as control groups (P < 0.05, P < 0.01), the penetration amount in the group of ES is markedly higher than DS group or control groups. Conversely, the retention contents of 5-FU and the fluorescence intensity of Rho in DS group were higher than those in ES group and control groups (P < 0.05, P < 0.01). In conclusion, both ES and DS could deliver 5-FU into the hypertrophic scars effectively. ES has better permeability of 5-FU than DS, DS has higher entrapment efficiency of 5-FU, and more 5-FU deposition in hypertrophic scar than ES. We should select ES or DS encapsulated with 5-FU according to clinical demand for hypertrophic scar therapy.
机译:为了比较两者均包裹有5-氟尿嘧啶(5-FU),5-FU微粒体悬液(5-FU ES,81.74±9.37 nm)和5-FU可变形的囊泡的脂质体和可变形脂质体之间的瘢痕穿透效率和保留率分别采用头投法和Cevc法制备脂质体悬浮液(5-FU DS,73.7±9.45 nm),通过粒度仪(PSS)确定其大小,并通过超速离心和微柱离心法检测其包封率(EE)。他们的透皮递送实验是在肥厚性瘢痕中进行的。 5-FU的渗透量和5-FU的保留含量均通过高效液相色谱法(HPLC)计算。通过激光扫描显微镜(LSM)测量用Rodanmin 6GO(Rho)标记的ES和DS的荧光强度。对照组为5-FU和空的核糖体囊泡(5-FU + EEV),5-FU和空的可变形脂质体囊泡(5-FU + EDV)和5-FU PBS溶液(5-FU Sol)建立。结果表明,制备的5-FU ES的尺寸为81.74±9.37nm,5-FU DS的为73.7±9.45nm,5-FU ES的EE为10.95%,5-FU DS的EE为15.05%。 5-FU ES组在24小时内,疤痕中5-FU的渗透量为14.12±0.1μg/ mL / cm〜2,5-FU的保留含量为10.74±1.17μg/ cm〜2 ,肥厚性瘢痕组织中Rho的荧光强度为182±18.3。在5-FU DS组中,5-FU的渗透量为12.35±1.21μg/ mL / cm〜2; 5-FU的保留含量为17.48±0.82μg/ cm〜2,Rho的荧光强度为241.45±7.63。 5-FU ES组与5-FU DS组以及对照组的渗透量之间存在统计学差异(P <0.05,P <0.01),ES组的渗透量显着高于DS组或对照组。相反,DS组的5-FU保留含量和Rho的荧光强度高于ES组和对照组(P <0.05,P <0.01)。总之,ES和DS均可有效地将5-FU递送至肥厚性瘢痕中。 ES比DS具有更好的5-FU渗透性,DS比ES具有更高的5-FU包封率,以及在肥厚性瘢痕中更多的5-FU沉积。根据肥厚性瘢痕治疗的临床需求,应选择5-FU包裹的ES或DS。

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