Evidence map›Paper›PMID 38266590›Full record

ArticleUltrasonics sonochemistry2024

Antisolvent fabrication of monodisperse liposomes using novel ultrasonic microreactors: Process optimization, performance comparison and intensification effect.

Caihe Peng, Xiaojing Zhu, Jie Zhang, Wenzhong Zhao, Jingfu Jia, Zhilin Wu, Zhixin Yu, Zhengya Dong

Abstract read
In one paragraph

Article in Ultrasonics sonochemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Ultrafine Ru-M Alloy@S Vacancy-Rich MoSAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Caihe PengSchool of Pharmacy, Changchun University of Chinese Medicine, 130117 Changchun, China.
Xiaojing ZhuChemistry and Chemical Engineering Guangdong Laboratory, 515031 Shantou, China. Electronic address: zhuxj@ccelab.com.cn.
Jie ZhangChemistry and Chemical Engineering Guangdong Laboratory, 515031 Shantou, China.
Wenzhong ZhaoLa Fang Jahwa Co., Ltd., 515144 Shantou, China.
Jingfu JiaChemistry and Chemical Engineering Guangdong Laboratory, 515031 Shantou, China.
Zhilin WuChemistry and Chemical Engineering Guangdong Laboratory, 515031 Shantou, China; College of Chemistry and Chemical Engineering, Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, 515063 Shantou, China.
Zhixin YuSchool of Pharmacy, Changchun University of Chinese Medicine, 130117 Changchun, China. Electronic address: yuzx01@ccucm.edu.cn.
Zhengya DongChemistry and Chemical Engineering Guangdong Laboratory, 515031 Shantou, China; College of Chemistry and Chemical Engineering, Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, 515063 Shantou, China; MoGe um-Flow Technology Co., Ltd., 515031 Shantou, China. Electronic address: zydong@ccelab.com.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liposomes as drug carriers for the delivery of therapeutic agents have triggered extensive research but it remains a grand challenge to develop a novel technology for enabling rapid and mass fabrication of monodisperse liposomes. In this work, we constructed a novel ultrasonic microfluidic technology, namely ultrasonic microreactor (USMR) with two different conjunction structure (co-flow and impinge flow, corresponding to USMR-CF and USMR-IF, respectively), to prepare uniform liposomes by antisolvent precipitation method. In this process, the monodisperse liposomes with tunable droplet sizes (DS) in 60-100 nm and a polydispersity index (PDI) less than 0.1 can easily be achieved by tuning the total flow rate, flow rate ratio, ultrasonic power, and lipid concentration within the two USMRs. Impressively, the USMR-IF is superior for reducing the PDI and tuning DS of the liposomes over the USMR-CF. More importantly, the ultrasonic can effectively reduce DS and PDI at the low TFR and support the IF-micromixer in reducing the PDI even at a high TFR. These remarkable performances are mainly due to the rapid active mixing, fouling-free property and high operation stability for USMR-IF. In addition, diverse lipid formulations can also be uniformly assembled into small liposomes with narrow distribution, such as the prepared HSPC-based liposome with DS of 59.6 nm and PDI of 0.08. The liposomes show a high stability and the yield can reach a high throughput with 108 g/h by using the USMR-IF at an initial lipid concentration of 60 mM. The results in the present work highlight a novel ultrasonic microfluidic technology in the preparation of liposomes and may pave an avenue for the rapid, fouling-free, and high throughput fabrication of different and monodisperse nanomedicines with controllable sizes and narrow distribution.

Indexed as

LiposomesUltrasonicsDrug CarriersLipidsMicrofluidicsParticle SizeDrug CarriersLipidsLiposomesCo-flowHigh throughputImpinge flowMonodisperse liposomesUltrasonic microreactor

Identifiers

PMID38266590
PMCPMC10818068

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.