Unraveling the surface marker signature of cell-derived vesicles via proteome analysis and nanoparticle flow cytometry DOI Creative Commons

Hui-Chong Lau,

Ilaria Passalacqua,

Jik‐Han Jung

и другие.

Research Square (Research Square), Год журнала: 2023, Номер unknown

Опубликована: Окт. 10, 2023

Abstract The cell-derived vesicles (CDVs) obtained using a proprietary extrusion process are the foundation of BioDrone™ platform technology. With superior productivity and versatility, this technology has garnered increasing attention in broad applications, particularly as drug delivery vehicle. Previously, we showed that CDVs exhibited varying levels expression for tetraspanin organelle membrane markers while revealing no discernible differences physical characteristics compared to naturally produced extracellular (EVs). To further understand utilize therapeutic potentials CDVs, more comprehensive study protein profiles is necessary. In addition, it crucial validate from indeed intact lipid rather than other impurities. Here, multiple batches EVs HEK293 cells. were subjected same purification processes subsequent proteome particle analyses. analyses revealed unique signatures between EVs, parental Extensive identified nine most prominent abundant cells EVs. Subsequent western blotting nanoparticle flow cytometry confirmed CD63, lysosome-associated glycoprotein 1 (LAMP1), nicastrin (NCSTN) highly enriched whereas CD81, CD9, prostaglandin F2 receptor negative regulator (PTGFRN) This highlights composition marker signature distinct Lastly, demonstrated 90% genuine by combining two different classes vesicle labeling dyes detergents disrupt membranes. indicates our compatible with well-characterized EV production methods. robust CDV will also facilitate engineering achieve enhanced effects or tissue-selective cargo delivery.

Язык: Английский

Brief Comparison of the Efficacy of Cationic and Anionic Liposomes as Nonviral Delivery Systems DOI Creative Commons

Carlos Ochoa-Sánchez,

Ericka Rodríguez-León, Ramón Íñiguez-Palomares

и другие.

ACS Omega, Год журнала: 2024, Номер 9(47), С. 46664 - 46678

Опубликована: Ноя. 13, 2024

In recent decades, the development and application of nonviral vectors, such as liposomes lipidic nanoparticles, for gene therapy drug delivery have seen substantial progress. The interest in physicochemical properties structures complexes liposome/DNA liposome/RNA is due to their potential substitute viruses carriers drugs or genetic material into cells with minimal cytotoxicity, which could lead use therapy. Initially, cationic were utilized DNA vectors; subsequently, different molecules, polymers, incorporated enhance transfection efficiency. Additionally, liposome/protein been developed vectors treatment diseases. most relevant internalization pathways these few results obtained using targeted nontargeted are discussed below. high cytotoxicity represents a significant challenge delivery. Anionic offer promising alternative address limitations conventional liposomes, including immune response, short circulation time, low toxicity. This review will discuss advantages novel anionic liposome-based systems that emerged result. advent designs manufacturing techniques has facilitated innovative systems, designated lipid nanoparticles (LNPs), serve highly efficacious regulators system.

Язык: Английский

Процитировано

2

Harnessing the potential of aptamers in cell-derived vesicles for targeting colorectal cancers at Pan-Dukes' stages DOI

Eun Sung Lee,

Byung Seok,

Young Jun Jang

и другие.

International Journal of Biological Macromolecules, Год журнала: 2024, Номер unknown, С. 135911 - 135911

Опубликована: Сен. 1, 2024

Язык: Английский

Процитировано

0

Engineered Cell‐Derived Nanovesicles with CAR and PH20 for Enhanced Targeted Photodynamic Cancer Therapy and Tumor Microenvironment Modulation DOI Open Access
Hongjun Oh, Gye Ryeol Park, Jieun Han

и другие.

Advanced Functional Materials, Год журнала: 2024, Номер unknown

Опубликована: Дек. 31, 2024

Abstract Photodynamic therapy (PDT) is a promising cancer treatment, but its clinical use limited by nontargeted photosensitizers (PS) that accumulate in normal tissues, causing adverse effects, and poor penetration tumor tissues due to the dense extracellular matrix (ECM). Here an innovative approach presented using cell‐derived nanovesicles (CNVs) engineered with chimeric antigen receptor (CAR) hyaluronidase PH20 enhance targeted PDT. The CAR–PH20 CNVs, loaded photosensitizer pheophorbide (PheoA), specifically target HER2‐expressing cells degrade hyaluronic acid microenvironment (TME), improving drug distribution. In vitro vivo experiments demonstrate increased reactive oxygen species (ROS) generation, improved retention, enhanced therapeutic efficacy compared conventional methods. When combined laser irradiation, these CNVs induce significant cell apoptosis inhibit growth mouse models, while minimizing toxicity tissues. This platform offers strategy for targeted, TME‐modulating PDT efficacy, reduced side marking advance nanodrug‐based therapies.

Язык: Английский

Процитировано

0

Unraveling the surface marker signature of cell-derived vesicles via proteome analysis and nanoparticle flow cytometry DOI Creative Commons

Hui-Chong Lau,

Ilaria Passalacqua,

Jik‐Han Jung

и другие.

Research Square (Research Square), Год журнала: 2023, Номер unknown

Опубликована: Окт. 10, 2023

Abstract The cell-derived vesicles (CDVs) obtained using a proprietary extrusion process are the foundation of BioDrone™ platform technology. With superior productivity and versatility, this technology has garnered increasing attention in broad applications, particularly as drug delivery vehicle. Previously, we showed that CDVs exhibited varying levels expression for tetraspanin organelle membrane markers while revealing no discernible differences physical characteristics compared to naturally produced extracellular (EVs). To further understand utilize therapeutic potentials CDVs, more comprehensive study protein profiles is necessary. In addition, it crucial validate from indeed intact lipid rather than other impurities. Here, multiple batches EVs HEK293 cells. were subjected same purification processes subsequent proteome particle analyses. analyses revealed unique signatures between EVs, parental Extensive identified nine most prominent abundant cells EVs. Subsequent western blotting nanoparticle flow cytometry confirmed CD63, lysosome-associated glycoprotein 1 (LAMP1), nicastrin (NCSTN) highly enriched whereas CD81, CD9, prostaglandin F2 receptor negative regulator (PTGFRN) This highlights composition marker signature distinct Lastly, demonstrated 90% genuine by combining two different classes vesicle labeling dyes detergents disrupt membranes. indicates our compatible with well-characterized EV production methods. robust CDV will also facilitate engineering achieve enhanced effects or tissue-selective cargo delivery.

Язык: Английский

Процитировано

0