Soluplus-stabilized 5-fluorouracil-entrapped niosomal formulations prepared via active and passive loading techniques: comparative physico-chemical evaluation

尼奥体 分散性 傅里叶变换红外光谱 粒径 化学 材料科学 动态光散射 化学工程 粒度分布 药物输送 小泡 纳米颗粒 色谱法 纳米技术 有机化学 生物化学 物理化学 工程类
作者
Onyinyechi Lydia Ugorji,Olisa Ivy Okoye,Chinekwu Nwangwu,Chinazom Precious Agbo,Franklin C. Kenechukwu
出处
期刊:Journal of Dispersion Science and Technology [Taylor & Francis]
卷期号:45 (5): 891-899 被引量:1
标识
DOI:10.1080/01932691.2023.2186427
摘要

AbstractAbstractThe objective of this study was to prepare and conduct a comparative analysis on 5-fluorouracil (5FU) niosomes stabilized with or without Soluplus, utilizing, respectively, passive loading and active loading techniques. Cholesterol was combined with Span 40 and Tween 40 surfactants to prepare several niosomal formulations by either passive or active methods. Encapsulation efficiency (EE%), loading capacity (LC), mean particle sizes, polydispersity indices (PDI), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), pH stability, and in vitro drug release in bio relevant media of pH 1.2, 6.8, and 7.4 were employed to evaluate the formulations. Batches made using the active loading approach (B1-B5) demonstrated higher entrapment efficiency (25–40%) (p ˂ 0.05) than those made using the passive loading method (20%) (with the exception of batch A1). In comparison to niosomes made using the passive loading method, the active loading methodology produced niosomes with a lower PDI (˂ 0.25) and particle size (˂ 70 nm). SEM revealed spherical and discrete vesicles for the Soluplus stabilized niosomes. Both approaches produced niosomes with prominent hydrogen bonding as observed in the FTIR study. The formulations were stable and sustained drug release, but the active loading strategy imparted a more sustained release pattern than the passively loaded one. Soluplus stabilized niosomes demonstrated higher (p ˂ 0.05) drug release (60–70%) in all release media. Based on the production of smaller particle sizes and narrower size distribution, the active loading strategy may be a more effective way to load hydrophilic medicines such as 5FU into niosomes.Graphical AbstractKeywords: Soluplusactive loadingpassive loading5-flourouracilniosomescomparative evaluation AcknowlegdmentWe want to acknowledge Prof N.C. Obitte for the kind provision of Soluplus used in this study.Conflict of interestThe authors have no conflict of interest to declare.Additional informationFundingThere was no funding for this research
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
4秒前
游戏人间完成签到 ,获得积分10
5秒前
shanika完成签到,获得积分10
5秒前
6秒前
清茶完成签到,获得积分10
6秒前
Bonnie发布了新的文献求助10
6秒前
vousme完成签到 ,获得积分10
6秒前
7秒前
9秒前
9秒前
9秒前
情怀应助顺利的凡蕾采纳,获得10
9秒前
17发布了新的文献求助10
10秒前
念姬发布了新的文献求助10
12秒前
14秒前
王美美发布了新的文献求助10
14秒前
14秒前
15秒前
欧阳正义发布了新的文献求助10
15秒前
初遇之时最暖完成签到,获得积分10
15秒前
噗噗发布了新的文献求助10
16秒前
天天快乐应助xy采纳,获得10
18秒前
rx发布了新的文献求助10
19秒前
Owen应助哈哈公子25采纳,获得10
20秒前
柯一一应助flysky120采纳,获得10
20秒前
zy发布了新的文献求助50
21秒前
21秒前
ZhijunXiang发布了新的文献求助10
21秒前
王美美完成签到,获得积分20
22秒前
22秒前
向日葵完成签到,获得积分10
22秒前
23秒前
fenmiao发布了新的文献求助10
24秒前
赘婿应助科研通管家采纳,获得10
24秒前
yookia应助科研通管家采纳,获得10
24秒前
共享精神应助科研通管家采纳,获得10
24秒前
yookia应助科研通管家采纳,获得10
24秒前
乐乐应助科研通管家采纳,获得10
24秒前
彭于晏应助科研通管家采纳,获得10
25秒前
高分求助中
A new approach to the extrapolation of accelerated life test data 1000
Cognitive Neuroscience: The Biology of the Mind 1000
Technical Brochure TB 814: LPIT applications in HV gas insulated switchgear 1000
Immigrant Incorporation in East Asian Democracies 600
Nucleophilic substitution in azasydnone-modified dinitroanisoles 500
不知道标题是什么 500
A Preliminary Study on Correlation Between Independent Components of Facial Thermal Images and Subjective Assessment of Chronic Stress 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3966726
求助须知:如何正确求助?哪些是违规求助? 3512179
关于积分的说明 11162302
捐赠科研通 3247077
什么是DOI,文献DOI怎么找? 1793689
邀请新用户注册赠送积分活动 874549
科研通“疑难数据库(出版商)”最低求助积分说明 804429