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A comparative study: the prospective influence of nanovectors in leveraging the chemopreventive potential of COX-2 inhibitors against skin cancer.
- Source :
-
International journal of nanomedicine [Int J Nanomedicine] 2019 Sep 17; Vol. 14, pp. 7561-7581. Date of Electronic Publication: 2019 Sep 17 (Print Publication: 2019). - Publication Year :
- 2019
-
Abstract
- Introduction: This study was conducted to elucidate the chemopreventive potential, cytotoxic, and suppression of cellular metastatic activity of etodolac (ETD)-loaded nanocarriers.<br />Methods: To esteem the effect of charge and composition of the nanovectors on their performance, four types of vectors namely, negative lipid nanovesicles; phosalosomes (N-Phsoms), positive phosalosomes (P-Phsoms), nanostructured lipid carriers (NLCs) and polymeric alginate polymer (AlgNPs) were prepared and compared. ETD was used as a model cyclo-oxygenase-2 (COX-2) inhibitor to evaluate the potency of these nanovectors to increase ETD permeation and retention through human skin and cytotoxicity against squamous cell carcinoma cell line (SCC). Moreover, the chemopreventive activity of ETD nanovector on mice skin cancer model was evaluated.<br />Results: Among the utilized nanovectors, ETD-loaded N-Phsoms depicted spherical vesicles with the smallest particle size (202.96±2.37 nm) and a high zeta potential of -24.8±4.16 mV. N-Phsoms exhibited 1.5, and 3.6 folds increase in the ETD amount deposited in stratum corneum, epidermis and dermis. Moreover, cytotoxicity studies revealed a significant cytotoxic potential of such nanovector with IC <subscript>50</subscript> =181.76 compared to free ETD (IC <subscript>50</subscript> =982.75), correlated to enhanced cellular internalization. Its efficacy extended to a reduction in the relative tumor weight with 1.70 and 1.51-fold compared to positive control and free ETD, that manifested by a 1.72-fold reduction in both COX-2 and proliferating cell nuclear antigen mRNA (PCNA-mRNA) levels and 2.63-fold elevation in caspase-3 level in skin tumors relative to the positive control group with no hepato-and nephrotoxicity.<br />Conclusion: Encapsulation of ETD in nanovector enhances its in-vitro and in-vivo anti-tumor activity and opens the door for encapsulation of more relevant drugs.<br />Competing Interests: The authors report no personal or financial conflicts of interest regarding this paper.<br /> (© 2019 Abo Aasy et al.)
- Subjects :
- Animals
Antineoplastic Agents pharmacology
Antineoplastic Agents therapeutic use
Cell Line, Tumor
Cell Survival drug effects
Cyclooxygenase 2 Inhibitors pharmacology
Cyclooxygenase 2 Inhibitors toxicity
Drug Carriers chemistry
Drug Liberation
Etodolac pharmacology
Etodolac therapeutic use
Female
Humans
Inhibitory Concentration 50
Lipids chemistry
Mice
Nanostructures ultrastructure
Particle Size
Prospective Studies
Skin Absorption drug effects
Skin Neoplasms pathology
Static Electricity
Treatment Outcome
Chemoprevention
Cyclooxygenase 2 metabolism
Cyclooxygenase 2 Inhibitors therapeutic use
Nanostructures chemistry
Skin Neoplasms drug therapy
Skin Neoplasms enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1178-2013
- Volume :
- 14
- Database :
- MEDLINE
- Journal :
- International journal of nanomedicine
- Publication Type :
- Academic Journal
- Accession number :
- 31571864
- Full Text :
- https://doi.org/10.2147/IJN.S218905