4.7 Article

Comparative Investigation of Cellular Effects of Polyethylene Glycol (PEG) Derivatives

Journal

POLYMERS
Volume 14, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/polym14020279

Keywords

Caco-2; MTT assay; NR assay; autophagy; flow cytometry; osmolality; G; mellonella

Funding

  1. Stipendium Hungaricum Scholarship
  2. Ministry for Innovation and Technology in Hungary [TKP2020-IKA-04]
  3. European Union
  4. European Regional Development Fund
  5. [GINOP-2.3.4-15-2020-00008]
  6. [GINOP-2.3.3-15-2016-0002]

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Polyethylene glycols (PEGs) are widely used in cosmetics, consumer care products, and the pharmaceutical industry due to their advantageous properties. However, little research has been done on the comparative study of PEGs with different molecular weights. This study aimed to investigate the effects of PEGs on cells and larvae, and correlate these effects with molecular weight and osmolality. The results showed that the effects of PEGs were correlated with their structure, molecular weight, osmolality, and cytotoxicity.
Nowadays, polyethylene glycols referred to as PEGs are widely used in cosmetics, consumer care products, and the pharmaceutical industry. Their advantageous properties such as chemical stability, low immunogenicity, and high tolerability explain why PEGs are applied in many fields of pharmaceutical formulations including parenteral, topical, ophthalmic, oral, and rectal preparations and also in modern drug delivery systems. Given their extensive use, they are considered a well-known group of chemicals. However, the number of large-scale comparative studies involving multiple PEGs of wide molecular weight range is low, as in most cases biological effects are estimated upon molecular weight. The aim of this publication was to study the action of PEGs on Caco-2 cells and G. mellonella larvae and to calculate the correlation of these effects with molecular weight and osmolality. Eleven PEGs of different molecular weight were used in our experiments: PEG 200, PEG 300, PEG 400, PEG 600, PEG 1000, PEG 1500, PEG 4000, PEG 8000, PEG 10,000, 12,000, and PEG 20,000. The investigated cellular effects included cytotoxicity (MTT and Neutral Red assays, flow cytometry with propidium iodide and annexin V) and autophagy. The osmolality of different molecular weight PEGs with various concentrations was measured by a vapor pressure osmometer OSMOMAT 070 and G. mellonella larvae were injected with the solutions of PEGs. Sorbitol was used as controls of the same osmolality. Statistical correlation was calculated to describe the average molecular weight dependence of the different measured effects. Osmolality, the cytotoxicity assays, flow cytometry data, and larvae mortality had significant correlation with the structure of the PEGs, while autophagosome formation and the proportion of early apoptotic cells showed no statistical correlation. Overall, it must be noted that PEGs must be tested individually for biological effects as not all effects can be estimated by the average molecular weight.

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