Carvacrol/β-cyclodextrin inclusion complex inhibits cell proliferation and migration of prostate cancer cells
Carvacrol, a phenolic monoterpene derived from thyme oil has gained wide interest recently because of its anticancer activities. To improve the solubility of carvacrol, the formation of inclusion complexes with β-cyclodextrin was performed by ultrasound and freeze-drying methods and characterized us...
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Published in | Food and chemical toxicology Vol. 125; pp. 198 - 209 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ltd
01.03.2019
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Abstract | Carvacrol, a phenolic monoterpene derived from thyme oil has gained wide interest recently because of its anticancer activities. To improve the solubility of carvacrol, the formation of inclusion complexes with β-cyclodextrin was performed by ultrasound and freeze-drying methods and characterized using thermal analysis, FTIR, XRD, SEM, NMR and HPLC analysis. From these results, carvacrol was successfully complexed within β-cyclodextrin cavity. Moreover, HPLC analysis demonstrated a higher entrapment efficiency for freeze-drying method (81.20 ± 0.52%) in contrast to ultrasound method (34.02 ± 0.67%). Hence, freeze-drying inclusion complex was evaluated for its antiproliferative effect and cytotoxicity against prostate cancer cell line (PC3) in vitro. Further, freeze-drying complex led to a dose-dependent inhibition in tumor cell growth in 2D and 3D cell culture systems. Altogether, the inclusion of carvacrol in β-cyclodextrin led to the formation of stable complexes with potent antiproliferative effects against PC3 cells, in vitro. Such an improved cytotoxic effect can be attributed to the enhanced the aqueous solubility and bioavailability of carvacrol by effective complexation in β-cyclodextrin.
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•CARV/β-CD complexes have been developed to improve the anticancer activity.•The FD method showed high efficiency in the formation of inclusion complexes.•FD complexes enhanced in vitro anticancer activity and cytotoxicity against PC3.•FD complex also reduced the cell viability of PC3 encapsulated in GelMA hydrogels. |
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AbstractList | Carvacrol, a phenolic monoterpene derived from thyme oil has gained wide interest recently because of its anticancer activities. To improve the solubility of carvacrol, the formation of inclusion complexes with β-cyclodextrin was performed by ultrasound and freeze-drying methods and characterized using thermal analysis, FTIR, XRD, SEM, NMR and HPLC analysis. From these results, carvacrol was successfully complexed within β-cyclodextrin cavity. Moreover, HPLC analysis demonstrated a higher entrapment efficiency for freeze-drying method (81.20 ± 0.52%) in contrast to ultrasound method (34.02 ± 0.67%). Hence, freeze-drying inclusion complex was evaluated for its antiproliferative effect and cytotoxicity against prostate cancer cell line (PC3) in vitro. Further, freeze-drying complex led to a dose-dependent inhibition in tumor cell growth in 2D and 3D cell culture systems. Altogether, the inclusion of carvacrol in β-cyclodextrin led to the formation of stable complexes with potent antiproliferative effects against PC3 cells, in vitro. Such an improved cytotoxic effect can be attributed to the enhanced the aqueous solubility and bioavailability of carvacrol by effective complexation in β-cyclodextrin. Carvacrol, a phenolic monoterpene derived from thyme oil has gained wide interest recently because of its anticancer activities. To improve the solubility of carvacrol, the formation of inclusion complexes with β-cyclodextrin was performed by ultrasound and freeze-drying methods and characterized using thermal analysis, FTIR, XRD, SEM, NMR and HPLC analysis. From these results, carvacrol was successfully complexed within β-cyclodextrin cavity. Moreover, HPLC analysis demonstrated a higher entrapment efficiency for freeze-drying method (81.20 ± 0.52%) in contrast to ultrasound method (34.02 ± 0.67%). Hence, freeze-drying inclusion complex was evaluated for its antiproliferative effect and cytotoxicity against prostate cancer cell line (PC3) in vitro. Further, freeze-drying complex led to a dose-dependent inhibition in tumor cell growth in 2D and 3D cell culture systems. Altogether, the inclusion of carvacrol in β-cyclodextrin led to the formation of stable complexes with potent antiproliferative effects against PC3 cells, in vitro. Such an improved cytotoxic effect can be attributed to the enhanced the aqueous solubility and bioavailability of carvacrol by effective complexation in β-cyclodextrin.Carvacrol, a phenolic monoterpene derived from thyme oil has gained wide interest recently because of its anticancer activities. To improve the solubility of carvacrol, the formation of inclusion complexes with β-cyclodextrin was performed by ultrasound and freeze-drying methods and characterized using thermal analysis, FTIR, XRD, SEM, NMR and HPLC analysis. From these results, carvacrol was successfully complexed within β-cyclodextrin cavity. Moreover, HPLC analysis demonstrated a higher entrapment efficiency for freeze-drying method (81.20 ± 0.52%) in contrast to ultrasound method (34.02 ± 0.67%). Hence, freeze-drying inclusion complex was evaluated for its antiproliferative effect and cytotoxicity against prostate cancer cell line (PC3) in vitro. Further, freeze-drying complex led to a dose-dependent inhibition in tumor cell growth in 2D and 3D cell culture systems. Altogether, the inclusion of carvacrol in β-cyclodextrin led to the formation of stable complexes with potent antiproliferative effects against PC3 cells, in vitro. Such an improved cytotoxic effect can be attributed to the enhanced the aqueous solubility and bioavailability of carvacrol by effective complexation in β-cyclodextrin. Carvacrol, a phenolic monoterpene derived from thyme oil has gained wide interest recently because of its anticancer activities. To improve the solubility of carvacrol, the formation of inclusion complexes with β-cyclodextrin was performed by ultrasound and freeze-drying methods and characterized using thermal analysis, FTIR, XRD, SEM, NMR and HPLC analysis. From these results, carvacrol was successfully complexed within β-cyclodextrin cavity. Moreover, HPLC analysis demonstrated a higher entrapment efficiency for freeze-drying method (81.20 ± 0.52%) in contrast to ultrasound method (34.02 ± 0.67%). Hence, freeze-drying inclusion complex was evaluated for its antiproliferative effect and cytotoxicity against prostate cancer cell line (PC3) in vitro. Further, freeze-drying complex led to a dose-dependent inhibition in tumor cell growth in 2D and 3D cell culture systems. Altogether, the inclusion of carvacrol in β-cyclodextrin led to the formation of stable complexes with potent antiproliferative effects against PC3 cells, in vitro. Such an improved cytotoxic effect can be attributed to the enhanced the aqueous solubility and bioavailability of carvacrol by effective complexation in β-cyclodextrin. [Display omitted] •CARV/β-CD complexes have been developed to improve the anticancer activity.•The FD method showed high efficiency in the formation of inclusion complexes.•FD complexes enhanced in vitro anticancer activity and cytotoxicity against PC3.•FD complex also reduced the cell viability of PC3 encapsulated in GelMA hydrogels. |
Author | Bertassoni, Luiz E. Bezerra, Daniel P. Shanmugam, Saravanan Araújo, Adriano A.S. França, Cristiane M. Carvalho, Yasmim M.B.G. Menezes, Paula P. Lima, Bruno S. Duarte, Marcelo C. Souza, Eloísa P.B.S.S. Thrivikraman, Greeshma Quintans-Júnior, Lucindo J. Trindade, Gabriela G.G. |
Author_xml | – sequence: 1 givenname: Gabriela G.G. surname: Trindade fullname: Trindade, Gabriela G.G. email: gabyggt@gmail.com organization: Department of Pharmacy, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil – sequence: 2 givenname: Greeshma surname: Thrivikraman fullname: Thrivikraman, Greeshma email: greeshmatnair@gmail.com organization: Division of Biomaterials and Biomechanics, Department of Restorative Dentistry, School of Dentistry, Oregon Health and Science University, Portland, OR, United States – sequence: 3 givenname: Paula P. orcidid: 0000-0002-4908-540X surname: Menezes fullname: Menezes, Paula P. email: paula.dp.menezes@gmail.com organization: Department of Pharmacy, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil – sequence: 4 givenname: Cristiane M. surname: França fullname: França, Cristiane M. email: cristiane321@gmail.com organization: Division of Biomaterials and Biomechanics, Department of Restorative Dentistry, School of Dentistry, Oregon Health and Science University, Portland, OR, United States – sequence: 5 givenname: Bruno S. surname: Lima fullname: Lima, Bruno S. email: brunolimafarm@gmail.com organization: Department of Pharmacy, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil – sequence: 6 givenname: Yasmim M.B.G. surname: Carvalho fullname: Carvalho, Yasmim M.B.G. email: yasmimgomess@gmail.com organization: Department of Pharmacy, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil – sequence: 7 givenname: Eloísa P.B.S.S. surname: Souza fullname: Souza, Eloísa P.B.S.S. email: eloisaportugal@gmail.com organization: Department of Pharmacy, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil – sequence: 8 givenname: Marcelo C. surname: Duarte fullname: Duarte, Marcelo C. email: duarte6cavalcante@gmail.com organization: Department of Pharmacy, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil – sequence: 9 givenname: Saravanan orcidid: 0000-0002-3781-8426 surname: Shanmugam fullname: Shanmugam, Saravanan email: saranflora04@gmail.com organization: Department of Pharmacy, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil – sequence: 10 givenname: Lucindo J. orcidid: 0000-0001-5155-938X surname: Quintans-Júnior fullname: Quintans-Júnior, Lucindo J. email: lucindojr@gmail.com organization: Department of Physiology, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil – sequence: 11 givenname: Daniel P. orcidid: 0000-0002-6774-2063 surname: Bezerra fullname: Bezerra, Daniel P. email: danielpbezerra@gmail.com organization: Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Bahia, Brazil – sequence: 12 givenname: Luiz E. surname: Bertassoni fullname: Bertassoni, Luiz E. email: bertasso@ohsu.edu organization: Division of Biomaterials and Biomechanics, Department of Restorative Dentistry, School of Dentistry, Oregon Health and Science University, Portland, OR, United States – sequence: 13 givenname: Adriano A.S. surname: Araújo fullname: Araújo, Adriano A.S. email: adriasa2001@yahoo.com.br organization: Department of Pharmacy, Federal University of Sergipe, São Cristóvão, Sergipe, Brazil |
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Keywords | Carvacrol Cell viability β-cyclodextrin Prostate cancer Inclusion complex |
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Snippet | Carvacrol, a phenolic monoterpene derived from thyme oil has gained wide interest recently because of its anticancer activities. To improve the solubility of... |
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SubjectTerms | antineoplastic activity beta-cyclodextrin bioavailability Carvacrol cell culture cell growth cell lines cell proliferation Cell viability cytotoxicity dose response Fourier transform infrared spectroscopy freeze drying high performance liquid chromatography Inclusion complex monoterpenoids neoplasm cells nuclear magnetic resonance spectroscopy Prostate cancer prostatic neoplasms scanning electron microscopy solubility thermal analysis thyme oil toxicology X-ray diffraction β-cyclodextrin |
Title | Carvacrol/β-cyclodextrin inclusion complex inhibits cell proliferation and migration of prostate cancer cells |
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