Background: Liposome particles with smaller sizes could increase transdermal drug delivery efficacy for enhanced skin penetration. While microfluidic methods have enabled controlled liposome synthesis, achieving efficient production of ultrasmall nanoliposomes (NLP) with a size smaller than 40 nm yet remains an unmet challenge.
Methods: In this study, we employed a helical-blade-strengthened co-flow focusing (HBSCF) device to efficiently synthesize NLP, which demonstrated superior skin permeation and retention.
Results: Liposome formulation primarily contains unsaturated lecithin, which endows an unprecedented capacity to NLP to scavenge reactive oxygen species (ROS). Moreover, NLP can effectively encapsulate a broad spectrum of anti-aging agents, including coenzyme Q10 (CoQ10), while preserving its physical properties. In a photoaged skin model, topical application of CoQ10-loaded NLP (CoQ10@NLP) inhibited ultraviolet B (UVB)-induced matrix metalloproteinase-1 (MMP-1) production, and promoted collagen type I (Col-I) synthesis in skin cells, thereby effectively rejuvenating the photoaged skin.
Conclusions: This study presents a straightforward and efficient method for the production of NLP, thereby offering a promising platform for transdermal delivery of diverse therapeutic agents.
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http://dx.doi.org/10.3390/biomedicines13020322 | DOI Listing |
J Colloid Interface Sci
March 2025
School of Chinese Medicine, Shenyang Medical College, Shenyang 110034 Liaoning, China. Electronic address:
Electrocatalytic hydrogen evolution reaction (HER) via water splitting is a prospective technology for achieving the sustainable production of hydrogen. So, ruthenium-based electrocatalysts have been extensively studied. However, metallic ruthenium tends to agglomerate due to the high cohesive energy, resulting in decreased HER performance in practical usage.
View Article and Find Full Text PDFNat Commun
March 2025
School of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Late-stage and advanced colorectal cancer (CRC) often prove to be resistant to current treatment regimens, due to the evolving tumor microenvironment. Chemotherapy-dominated multi-modal therapeutic strategies based on the specific CRC microenvironment open a new horizon for eradicating colorectal tumors. Here, in situ valence-transited arsenic nanosheets are developed as a multi-modal therapeutic platform by responding to the HS-enriched CRC microenvironment.
View Article and Find Full Text PDFBiomedicines
January 2025
School of Chemistry and Materials Science, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou 310024, China.
Background: Liposome particles with smaller sizes could increase transdermal drug delivery efficacy for enhanced skin penetration. While microfluidic methods have enabled controlled liposome synthesis, achieving efficient production of ultrasmall nanoliposomes (NLP) with a size smaller than 40 nm yet remains an unmet challenge.
Methods: In this study, we employed a helical-blade-strengthened co-flow focusing (HBSCF) device to efficiently synthesize NLP, which demonstrated superior skin permeation and retention.
Innovation (Camb)
February 2025
Key Laboratory for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, University of Chinese Academy of Sciences, Beijing 100049, China.
We developed magnetically driven bionic drug-loaded nanorobots (MDNs) to accurately target tumors and deliver chemotherapy agents using a customized three-dimensional (3D) magnetic manipulation platform (MMP) system to precisely control their movement mode. MDNs were based on polyethylene glycol-modified homogeneous ultrasmall iron oxide nanoparticles (7.02 ± 0.
View Article and Find Full Text PDFTheranostics
February 2025
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
As substitutes for natural enzymes, nanozymes offer tunable enzyme-like activities and remarkable structural stability, granting them the potential to treat various diseases, including renal ischemia-reperfusion (I/R) injury. However, the majority of developed nanozymes suffer from unclear structures and limited activity profiles, which hinder the study of their structure-activity relationships, catalytic diversity, mass production, and clinical application. Herein, we introduce an atomically precise and ultrasmall cascade nanozyme based on a radical-functionalized metal-organic cage (MOC-R).
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