In vitro safety and efficacy evaluations of a complex botanical mixture of Eugenia dysenterica DC. (Myrtaceae): Prospects for developing a new dermocosmetic product

In the context of developing a new natural product-based cosmetic, the in vitro efficacy and safety evaluations of a complex botanical mixture based on Eugenia dysenterica leaf hydroalcoholic extract (EDE) (2.5–1000μg/mL) were carried out. Chromatographic analysis demonstrated the presence of the ta...

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Published inToxicology in vitro Vol. 45; no. Pt 3; pp. 397 - 408
Main Authors Moreira, Larissa Cleres, de Ávila, Renato Ivan, Veloso, Danillo Fabrini Maciel Costa, Pedrosa, Tatiana Nascimento, Lima, Emerson Silva, do Couto, Renê Oliveira, Lima, Eliana Martins, Batista, Aline Carvalho, de Paula, José Realino, Valadares, Marize Campos
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Published England Elsevier Ltd 01.12.2017
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Abstract In the context of developing a new natural product-based cosmetic, the in vitro efficacy and safety evaluations of a complex botanical mixture based on Eugenia dysenterica leaf hydroalcoholic extract (EDE) (2.5–1000μg/mL) were carried out. Chromatographic analysis demonstrated the presence of the tannin (ellagic acid) and flavonoids (quercetin and gallic acid) which characterize the EDE as a polyphenol-rich mixture. Using HFF-1 fibroblasts, it was shown that EDE promoted cell regeneration after UVA exposure. It also led to the inhibition of the collagenase, elastase and tyrosinase enzymes, which are involved in skin-related disorders. In terms of toxicological evaluation, the EDE was classified as non-phototoxic through the 3T3 Neutral Red Uptake Phototoxicity Test (OECD N° 432, 2004) and non-eye irritant by Bovine Corneal Opacity and Permeability (OECD N° 437, 2013) assay, in conjunction with corneal histomorphometric analysis. Furthermore, the EDE has no skin sensitization potential as demonstrated by a two-out-of-three prediction model [protein-binding/haptenization (OECD N° 442C, 2015), keratinocyte and dendritic cell activations]. In addition, it was shown that the EDE seems to be non-genotoxic through the cytokinesis-block micronucleus assay (OECD N° 487, 2014) using HepG2 cells. When considered together, these findings support the use of EDE botanical mixture in cosmetic/pharmaceutical products. •EDE is a polyphenol-rich complex botanical mixture containing ellagic acid, quercetin and gallic acid.•EDE exerts cell regeneration of HFF-1 fibroblasts after UVA exposure.•EDE has potential skin-whitening and anti-aging properties.•EDE seems to be well-tolerated topically, without any relevant toxic effects.
AbstractList In the context of developing a new natural product-based cosmetic, the in vitro efficacy and safety evaluations of a complex botanical mixture based on Eugenia dysenterica leaf hydroalcoholic extract (EDE) (2.5-1000μg/mL) were carried out. Chromatographic analysis demonstrated the presence of the tannin (ellagic acid) and flavonoids (quercetin and gallic acid) which characterize the EDE as a polyphenol-rich mixture. Using HFF-1 fibroblasts, it was shown that EDE promoted cell regeneration after UVA exposure. It also led to the inhibition of the collagenase, elastase and tyrosinase enzymes, which are involved in skin-related disorders. In terms of toxicological evaluation, the EDE was classified as non-phototoxic through the 3T3 Neutral Red Uptake Phototoxicity Test (OECD N° 432, 2004) and non-eye irritant by Bovine Corneal Opacity and Permeability (OECD N° 437, 2013) assay, in conjunction with corneal histomorphometric analysis. Furthermore, the EDE has no skin sensitization potential as demonstrated by a two-out-of-three prediction model [protein-binding/haptenization (OECD N° 442C, 2015), keratinocyte and dendritic cell activations]. In addition, it was shown that the EDE seems to be non-genotoxic through the cytokinesis-block micronucleus assay (OECD N° 487, 2014) using HepG2 cells. When considered together, these findings support the use of EDE botanical mixture in cosmetic/pharmaceutical products.
In the context of developing a new natural product-based cosmetic, the in vitro efficacy and safety evaluations of a complex botanical mixture based on Eugenia dysenterica leaf hydroalcoholic extract (EDE) (2.5–1000μg/mL) were carried out. Chromatographic analysis demonstrated the presence of the tannin (ellagic acid) and flavonoids (quercetin and gallic acid) which characterize the EDE as a polyphenol-rich mixture. Using HFF-1 fibroblasts, it was shown that EDE promoted cell regeneration after UVA exposure. It also led to the inhibition of the collagenase, elastase and tyrosinase enzymes, which are involved in skin-related disorders. In terms of toxicological evaluation, the EDE was classified as non-phototoxic through the 3T3 Neutral Red Uptake Phototoxicity Test (OECD N° 432, 2004) and non-eye irritant by Bovine Corneal Opacity and Permeability (OECD N° 437, 2013) assay, in conjunction with corneal histomorphometric analysis. Furthermore, the EDE has no skin sensitization potential as demonstrated by a two-out-of-three prediction model [protein-binding/haptenization (OECD N° 442C, 2015), keratinocyte and dendritic cell activations]. In addition, it was shown that the EDE seems to be non-genotoxic through the cytokinesis-block micronucleus assay (OECD N° 487, 2014) using HepG2 cells. When considered together, these findings support the use of EDE botanical mixture in cosmetic/pharmaceutical products. •EDE is a polyphenol-rich complex botanical mixture containing ellagic acid, quercetin and gallic acid.•EDE exerts cell regeneration of HFF-1 fibroblasts after UVA exposure.•EDE has potential skin-whitening and anti-aging properties.•EDE seems to be well-tolerated topically, without any relevant toxic effects.
In the context of developing a new natural product-based cosmetic, the in vitro efficacy and safety evaluations of a complex botanical mixture based on Eugenia dysenterica leaf hydroalcoholic extract (EDE) (2.5–1000 μg/mL) were carried out. Chromatographic analysis demonstrated the presence of the tannin (ellagic acid) and flavonoids (quercetin and gallic acid) which characterize the EDE as a polyphenol-rich mixture. Using HFF-1 fibroblasts, it was shown that EDE promoted cell regeneration after UVA exposure. It also led to the inhibition of the collagenase, elastase and tyrosinase enzymes, which are involved in skin-related disorders. In terms of toxicological evaluation, the EDE was classified as non-phototoxic through the 3T3 Neutral Red Uptake Phototoxicity Test (OECD N° 432, 2004) and non-eye irritant by Bovine Corneal Opacity and Permeability (OECD N° 437, 2013) assay, in conjunction with corneal histomorphometric analysis. Furthermore, the EDE has no skin sensitization potential as demonstrated by a two-out-of-three prediction model [protein-binding/haptenization (OECD N° 442C, 2015), keratinocyte and dendritic cell activations]. In addition, it was shown that the EDE seems to be non-genotoxic through the cytokinesis-block micronucleus assay (OECD N° 487, 2014) using HepG2 cells. When considered together, these findings support the use of EDE botanical mixture in cosmetic/pharmaceutical products.
Author Lima, Eliana Martins
Moreira, Larissa Cleres
de Paula, José Realino
Pedrosa, Tatiana Nascimento
de Ávila, Renato Ivan
Lima, Emerson Silva
Batista, Aline Carvalho
Valadares, Marize Campos
Veloso, Danillo Fabrini Maciel Costa
do Couto, Renê Oliveira
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  givenname: Danillo Fabrini Maciel Costa
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  givenname: Tatiana Nascimento
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  givenname: Renê Oliveira
  surname: do Couto
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  givenname: Eliana Martins
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  fullname: Lima, Eliana Martins
  organization: Laboratory of Pharmaceutical Technology - FarmaTec, Faculty of Pharmacy, Federal University of Goiás, Goiânia, GO, Brazil
– sequence: 8
  givenname: Aline Carvalho
  surname: Batista
  fullname: Batista, Aline Carvalho
  organization: Laboratory of Oral Pathology, Dental School, Federal University of Goiás, Goiânia, GO, Brazil
– sequence: 9
  givenname: José Realino
  surname: de Paula
  fullname: de Paula, José Realino
  organization: Laboratory of Natural Products Research - LPPN, Faculty of Pharmacy, Federal University of Goiás, Goiânia, GO, Brazil
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  givenname: Marize Campos
  surname: Valadares
  fullname: Valadares, Marize Campos
  email: marizeufg@gmail.com, marizecv@ufg.br
  organization: Laboratory of Celullar Toxicology and Pharmacology - FarmaTec, Faculty of Pharmacy, Federal University of Goiás, Goiânia, GO, Brazil
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Issue Pt 3
Keywords Cosmetic
MPE
CBPI
EDE
mDPRA
MNvit test-cytoB
SPF
DNCB
ITS
Skin-whitening
NRU
Risk evaluation
OD
SI
IC50
l-DOPA
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OMC
Anti-aging
Alternative methods
MUSST
PIF
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CV80
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Complex botanical mixture
BCOP
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Snippet In the context of developing a new natural product-based cosmetic, the in vitro efficacy and safety evaluations of a complex botanical mixture based on Eugenia...
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SubjectTerms Aging
Alternative methods
Animals
Anti-aging
Cattle
Cells, Cultured
Chromatography
Collagen
Collagenase
Complex botanical mixture
Complex Mixtures
Consumer Product Safety
Cornea
Cornea - drug effects
Cosmetic
Cosmetics
Cosmetics - chemistry
Cosmetics - toxicity
Cytokinesis
Dendritic cells
Dendritic Cells - drug effects
Dermatitis, Phototoxic
Dermatologic Agents - chemistry
Dermatologic Agents - toxicity
Elastase
Ellagic acid
Eugenia - chemistry
Eugenia - toxicity
Fibroblasts
Flavonoids
Gallic acid
Genotoxicity
Humans
Interleukin-18 - metabolism
Irritants - toxicity
Keratinocytes - drug effects
Mice
Micronucleus Tests
Natural products
Opacity
Permeability
Phototoxicity
Plant Extracts - chemistry
Plant Extracts - toxicity
Plant Leaves - chemistry
Product safety
Proteins
Quercetin
Regeneration
Risk evaluation
Risk factors
Skin
Skin-whitening
Tyrosinase
Ultraviolet radiation
Title In vitro safety and efficacy evaluations of a complex botanical mixture of Eugenia dysenterica DC. (Myrtaceae): Prospects for developing a new dermocosmetic product
URI https://dx.doi.org/10.1016/j.tiv.2017.04.002
https://www.ncbi.nlm.nih.gov/pubmed/28389280
https://www.proquest.com/docview/2090429243
https://search.proquest.com/docview/1885953073
Volume 45
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