One‐Step Formation of Targeted Liposomes in a Versatile Microfluidic Mixing Device

脂质体 光热治疗 微流控 纳米技术 材料科学 适体 荧光寿命成像显微镜 吲哚青绿 分子成像 显像剂 药物输送 疾病监测 体内 生物医学工程 荧光 医学 疾病 病理 生物技术 外科 物理 生物 量子力学 遗传学
作者
Shan Han,Xin Sun,Xin Liu,Qi Sun,Yao He,Ziyan Chen,Ziyan Chen,Qibo Lin,Zixi Jiang,Xiang Chen,Zeyu Chen,Zeyu Chen,Shuang Zhao
出处
期刊:Small [Wiley]
卷期号:19 (7): e2205498-e2205498 被引量:42
标识
DOI:10.1002/smll.202205498
摘要

Targeted liposomes, as a promising carrier, have received tremendous attention in COVID-19 vaccines, molecular imaging, and cancer treatment, due to their enhanced cellular uptake and payload accumulation at target sites. However, the conventional methods for preparing targeted liposomes still suffer from limitations, including complex operation, time-consuming, and poor reproducibility. Herein, a facile and scalable strategy is developed for one-step construction of targeted liposomes using a versatile microfluidic mixing device (MMD). The engineered MMD provides an advanced synthesis platform for multifunctional liposome with high production rate and controllability. To validate the method, a programmed death-ligand 1 (PD-L1)-targeting aptamer modified indocyanine green (ICG)-liposome (Apt-ICG@Lip) is successfully constructed via the MMD. ICG and the PD-L1-targeting aptamer are used as model drug and targeting moiety, respectively. The Apt-ICG@Lip has high encapsulation efficiency (89.9 ± 1.4%) and small mean diameter (129.16 ± 5.48 nm). In vivo studies (PD-L1-expressing tumor models) show that Apt-ICG@Lip can realize PD-L1 targeted photoacoustic imaging, fluorescence imaging, and photothermal therapy. To verify the versatility of this approach, various targeted liposomes with different functions are further prepared and investigated. These experimental results demonstrate that this method is concise, efficient, and scalable to prepare multifunctional targeted liposomal nanoplatforms for molecular imaging and disease theranostics.
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
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
四月想毕业完成签到,获得积分10
1秒前
huhaa发布了新的文献求助10
2秒前
2秒前
2秒前
xingyu发布了新的文献求助10
2秒前
3秒前
机灵的凉面完成签到,获得积分10
3秒前
英姑应助LXC采纳,获得10
3秒前
null应助科研通管家采纳,获得10
3秒前
小林子发布了新的文献求助10
3秒前
朝茗森完成签到,获得积分10
3秒前
3秒前
3秒前
乐乐应助科研通管家采纳,获得10
3秒前
酷酷的舞蹈完成签到,获得积分10
3秒前
华仔应助科研通管家采纳,获得10
3秒前
3秒前
张欢馨应助科研通管家采纳,获得10
3秒前
烟花应助科研通管家采纳,获得10
4秒前
jane发布了新的文献求助10
4秒前
张张完成签到,获得积分10
4秒前
4秒前
4秒前
Akim应助科研通管家采纳,获得10
4秒前
4秒前
null应助科研通管家采纳,获得10
4秒前
wanci应助科研通管家采纳,获得10
4秒前
爆米花应助科研通管家采纳,获得10
4秒前
catank应助科研通管家采纳,获得10
5秒前
gentle完成签到 ,获得积分10
5秒前
落寞的大凄完成签到,获得积分20
5秒前
852应助科研通管家采纳,获得10
5秒前
ding应助科研通管家采纳,获得10
5秒前
七七发布了新的文献求助10
5秒前
Nie发布了新的文献求助30
5秒前
5秒前
赘婿应助科研通管家采纳,获得10
5秒前
领导范儿应助科研通管家采纳,获得30
5秒前
5秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Römisch-Germanische Forschungen 1000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
Green Fire Retardants for Polymeric Materials 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7615835
求助须知:如何正确求助?哪些是违规求助? 9191066
关于积分的说明 19694880
捐赠科研通 7188362
什么是DOI,文献DOI怎么找? 3271457
关于科研通互助平台的介绍 2434611
邀请新用户注册赠送积分活动 2266528