Elongated Particles Show a Preferential Uptake in Invasive Cancer Cells

Mechanically driven cellular preference for drug carriers can enhance selectivity in cancer therapy, underscoring the importance of understanding the physical aspects of particle uptake. In this study, it was hypothesized that elongated particles might be preferentially taken up by deformable, aggre...

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Main Authors: Talya Cohen, Chalom Zemmour, Ora T. Cohen, Ofra Benny
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Nanomaterials
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Online Access:https://www.mdpi.com/2079-4991/14/23/1891
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author Talya Cohen
Chalom Zemmour
Ora T. Cohen
Ofra Benny
author_facet Talya Cohen
Chalom Zemmour
Ora T. Cohen
Ofra Benny
author_sort Talya Cohen
collection DOAJ
description Mechanically driven cellular preference for drug carriers can enhance selectivity in cancer therapy, underscoring the importance of understanding the physical aspects of particle uptake. In this study, it was hypothesized that elongated particles might be preferentially taken up by deformable, aggressive cancer cells compared to normal cells. Two film-stretching methods were tested for 0.8–2.4 μm polystyrene (PS) particles: one based on solubility in organic solvents and the other on heat-induced softening. The heat-induced method produced more homogenous particle batches, with a standard deviation in the particle aspect ratio of 0.42 compared to 0.91 in the solvent-based method. The ability of cells to engulf elongated PS particles versus spherical particles was assessed in two subsets of human melanoma A375 cells. In the more aggressive cancer cell subset (A375+), uptake of elongated PS particles increased by 10% compared to spherical particles. In contrast, the less aggressive subset (A375−) showed a 25% decrease in uptake of elongated particles. This resulted in an uptake ratio between A375+ and A375− that was 1.5 times higher for elongated PS particles than for spherical ones. To further demonstrate relevance to drug delivery, elongated paclitaxel-loaded biodegradable, slow-releasing poly(lactic-co-glycolic) acid (PLGA) particles were synthesized. No significant difference in cytotoxic effect was observed between A375+ and A375− cells treated with spherical drug-loaded particles. However, treatment with ellipsoidal particles led to a significantly enhanced cytotoxic effect in aggressive cells compared to less aggressive cells. These findings present promising directions for tailored cancer drug delivery and demonstrate the importance of particle physical properties in cellular uptake and drug delivery mechanisms.
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spelling doaj-art-b84624bd79cc414eb215e66cedaccfdb2025-08-20T02:38:39ZengMDPI AGNanomaterials2079-49912024-11-011423189110.3390/nano14231891Elongated Particles Show a Preferential Uptake in Invasive Cancer CellsTalya Cohen0Chalom Zemmour1Ora T. Cohen2Ofra Benny3Institute for Drug Research, The School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 9112001, IsraelInstitute for Drug Research, The School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 9112001, IsraelInstitute for Drug Research, The School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 9112001, IsraelInstitute for Drug Research, The School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Jerusalem 9112001, IsraelMechanically driven cellular preference for drug carriers can enhance selectivity in cancer therapy, underscoring the importance of understanding the physical aspects of particle uptake. In this study, it was hypothesized that elongated particles might be preferentially taken up by deformable, aggressive cancer cells compared to normal cells. Two film-stretching methods were tested for 0.8–2.4 μm polystyrene (PS) particles: one based on solubility in organic solvents and the other on heat-induced softening. The heat-induced method produced more homogenous particle batches, with a standard deviation in the particle aspect ratio of 0.42 compared to 0.91 in the solvent-based method. The ability of cells to engulf elongated PS particles versus spherical particles was assessed in two subsets of human melanoma A375 cells. In the more aggressive cancer cell subset (A375+), uptake of elongated PS particles increased by 10% compared to spherical particles. In contrast, the less aggressive subset (A375−) showed a 25% decrease in uptake of elongated particles. This resulted in an uptake ratio between A375+ and A375− that was 1.5 times higher for elongated PS particles than for spherical ones. To further demonstrate relevance to drug delivery, elongated paclitaxel-loaded biodegradable, slow-releasing poly(lactic-co-glycolic) acid (PLGA) particles were synthesized. No significant difference in cytotoxic effect was observed between A375+ and A375− cells treated with spherical drug-loaded particles. However, treatment with ellipsoidal particles led to a significantly enhanced cytotoxic effect in aggressive cells compared to less aggressive cells. These findings present promising directions for tailored cancer drug delivery and demonstrate the importance of particle physical properties in cellular uptake and drug delivery mechanisms.https://www.mdpi.com/2079-4991/14/23/1891cancer cellsPLGA particlesellipsoid particles
spellingShingle Talya Cohen
Chalom Zemmour
Ora T. Cohen
Ofra Benny
Elongated Particles Show a Preferential Uptake in Invasive Cancer Cells
Nanomaterials
cancer cells
PLGA particles
ellipsoid particles
title Elongated Particles Show a Preferential Uptake in Invasive Cancer Cells
title_full Elongated Particles Show a Preferential Uptake in Invasive Cancer Cells
title_fullStr Elongated Particles Show a Preferential Uptake in Invasive Cancer Cells
title_full_unstemmed Elongated Particles Show a Preferential Uptake in Invasive Cancer Cells
title_short Elongated Particles Show a Preferential Uptake in Invasive Cancer Cells
title_sort elongated particles show a preferential uptake in invasive cancer cells
topic cancer cells
PLGA particles
ellipsoid particles
url https://www.mdpi.com/2079-4991/14/23/1891
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