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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5217_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Also of interest
- •Contents
- •Part I: Introduction
- •1.1.2.3 Sustainability and future perspectives
- •1.2 Alkaloids, flavonoids, terpenoids, and other active compounds
- •1.2.1 Alkaloids
- •1.2.2 Flavonoids
- •1.2.3 Terpenoids
- •1.2.4 Other active compounds
- •1.3 Chemical structures and pharmacological effects
- •1.3.1 Chemical structures and effects of alkaloids
- •1.3.2 Chemical structures and effects of flavonoids
- •1.3.3 Chemical structures and effects of terpenoids
- •1.3.4 Structures and effects of other compounds
- •1.4.2 Flavonoids
- •1.4.3 Terpenoids
- •1.4.4 Other active compounds
- •1.5 Chemical structures and pharmacological effects
- •1.5.1 Chemical structures and effects of alkaloids
- •1.1 Introduction to medicinal and aromatic plants
- •1.1.1 Historical background
- •1.1.1.1 Historical background
- •1.1.2 Traditional and modern uses
- •1.1.2.1 Traditional uses
- •1.1.2.2 Modern uses
- •1.5.2 Chemical structures and effects of flavonoids
- •1.5.3 Chemical structures and effects of terpenoids
- •1.5.4 Structures and effects of other compounds
- •1.6 Aromatic plants in everyday life
- •1.6.1 The importance of essential oils and aromatherapy
- •1.6.2 Applications in the cosmetics and food industry
- •1.6.3 Food industry
- •1.7.1 Protection of endangered species
- •1.7.2 Sustainable harvesting methods
- •1.8.1 Protection of endangered species
- •1.8.1.1 Threats to endangered species
- •1.8.2 Conservation strategies
- •1.8.2.1 Protection of natural habitats (in situ conservation)
- •1.8.3 Participation of local communities
- •1.8.3.1 Education and awareness
- •1.8.3.2 International collaborations
- •1.8.3.3 Sustainable harvesting and trade
- •1.8.4 Sustainable harvesting methods
- •1.8.4.1 The importance of sustainable harvesting
- •1.8.4.2 Sustainable harvesting principles
- •1.8.4.3 Sustainable harvesting techniques
- •1.8.4.4 Monitoring and evaluating the harvesting process
- •1.8.4.5 The economic dimension of sustainable harvesting
- •1.8.4.6 International approaches and legal regulations
- •1.8.4.6.1 International approaches
- •1.8.4.6.2 Legal regulations
- •1.8.4.6.3 Protection of local communities and traditional knowledge
- •1.8.5 Many countries are protecting biodiversity
- •1.8.5.1 Global conservation efforts
- •1.8.5.2 Protected areas and conservation in natural habitats
- •1.8.5.3 Ex situ conservation and gene banks
- •1.9 Challenges and future prospects
- •1.9.1 Impacts of climate change
- •1.9.2 Genetic and biotechnological approaches
- •1.9.2.1 Protection of genetic diversity and breeding studies
- •1.9.2.2 Genomic and transcriptomic approaches
- •1.9.2.3 Culture tissue techniques
- •1.9.2.4 CRISPR/Cas9 technology
- •1.9.2.5 Metabolic engineering and synthetic biology
- •1.9.2.6 Bioinformatics and data analysis
- •1.10 Case studies and regional practices
- •1.10.1 Successful projects in specific regions
- •1.10.1.1 India: Ayurveda and biodiversity conservation projects
- •1.10.1.2 Brazil: sustainable collection projects in the Amazon forest
- •1.10.1.3 Turkey: protection and production of endemic plants
- •1.10.1.4 Africa: integration of local knowledge with modern practices
- •1.10.2.1 Documentation and protection of traditional knowledge
- •1.10.2.2 Scientific validation and application
- •1.10.2.3 Education and awareness
- •1.10.2.4 Patents and intellectual property rights
- •1.10.2.5 Public and private sector collaboration
- •1.11 Conclusions
- •References
- •2.1 Introduction
- •2.3.1 Plant selection
- •2.3.1.1 Random plant selection
- •2.3.1.2 Plant selection based on ethnopharmacology and traditional uses
- •2.3.1.3 Plant selection by HTS technologies
- •2.3.1.4 Plant selection through virtual screening
- •2.3.1.5 Phytochemical databases
- •2.3.2.1 Comminution and homogenization
- •2.3.3 Extraction
- •2.3.3.1 Conventional extraction techniques
- •2.3.3.2 Maceration
- •2.3.3.3 Infusion
- •2.3.3.4 Decoction
- •2.3.3.5 Percolation
- •2.3.3.13 Pressurized liquid extraction
- •2.3.3.14 Enzyme-assisted extraction
- •2.3.3.15 Solid-phase microextraction
- •2.3.3.6 Hydrodistillation and steam distillation
- •2.3.3.7 Soxhlet extraction
- •2.3.3.8 Advanced extraction techniques
- •2.3.3.9 Ultrasound-assisted extraction
- •2.3.3.10 Pulsed-electric field extraction
- •2.3.3.11 Microwave-assisted extraction
- •2.3.3.12 Supercritical extraction
- •2.3.3.16 Bioassay-guided fractionation of plant extracts
- •2.3.4 Isolation and purification
- •2.3.4.3 Gas chromatography (GC)
- •2.3.4.4 Column chromatography (CC)
- •2.3.4.5 Ion exchange chromatography (IEC)
- •2.3.5 Elucidation of the chemical structure
- •2.3.5.1 Nuclear magnetic resonance (NMR)
- •2.3.5.2 Mass spectrometry (MS) and high-resolution mass spectrometry (HRMS)
- •2.3.5.4 UV-visible spectroscopy
- •2.3.6 Evaluation of therapeutic efficacy with bioassays
- •2.3.7 Preclinical and clinical researches
- •2.3.8 Structural modifications and developing new analogues
- •2.4 The use of omics technologies in drug discovery and development
- •2.4.1 Genomics
- •2.4.2 Metabolomics
- •2.4.3 Proteomics
- •2.5 Future scope
- •2.6 Conclusion
- •References
- •3.1 Introduction
- •3.2 Bioactive compounds
- •3.2.1 Alkaloids
- •3.2.2 Terpenoids (terpenes)
- •3.2.3 Phenolics
- •3.3 Industrial importance of biological active compounds
- •3.4 Industrial use of MAPs
- •3.5 Essential oils
- •3.6 MAPs in the dye industry
- •3.6.1 Use of MAPs in the perfumery
- •3.6.2 Use of MAPs in cosmetics
- •3.6.3 Use of MAPs in plastic production
- •3.6.4 Other industrial applications
- •3.6.5 MAPs in energy production
- •3.6.6 MAPs in agricultural applications
- •3.7 Salt stress
- •3.7.1 Nutrient
- •3.7.2 Productivity
- •3.7.3 Photosynthesis
- •3.8 Drought stress
- •3.9 Heavy metals
- •3.10 Heat stress
- •3.11 Soil pH
- •3.12 Light intensity
- •3.13 Pest and disease management
- •3.14 Conclusion and future perspective
- •References
- •4.1 Introduction
- •4.2 Toxic compounds and their effects
- •4.2.1 Alkaloids
- •4.2.2 Glycosides
- •4.2.3 Essential oils
- •4.2.4 Saponins
- •4.2.5 Coumarins
- •4.3 Poisonous medicinal plants
- •4.3.1 Digitalis purpurea (foxglove)
- •4.3.2 Atropa belladonna (deadly nightshade)
- •4.3.3 Aconitum napellus (monkshood, aconite)
- •4.3.4 Conium maculatum (hemlock)
- •4.3.5 Nerium oleander (oleander)
- •4.3.6 Datura stramonium (jimsonweed)
- •4.3.7 Ricinus communis (castor bean)
- •4.3.8 Taxus baccata (English yew)
- •4.3.9 Hyoscyamus niger (black henbane)
- •4.3.10 Cicuta virosa (water hemlock)
- •4.3.11 Veratrum viride (false hellebore)
- •4.3.12 Helleborus niger (Christmas rose)
- •4.3.13 Mandragora officinarum (mandrake)
- •4.3.14 Ageratina altissima (white snakeroot)
- •4.3.15 Bryonia alba (white bryony)
- •4.3.16 Colchicum autumnale (autumn crocus)
- •4.3.17 Chelidonium majus Linn. – Papaveraceae
- •4.4 Aromatic plants and poisons
- •4.4.1 Artemisia absinthium (wormwood)
- •4.4.2 Sassafras albidum (sassafras)
- •4.4.3 Lavandula angustifolia (lavender)
- •4.4.4 Rosmarinus officinalis (rosemary)
- •4.4.5 Mentha pulegium (pennyroyal)
- •4.4.6 Eucalyptus globulus (eucalyptus)
- •4.4.7 Myristica fragrans (nutmeg)
- •4.4.8 Thuja occidentalis (white cedar)
- •4.4.9 Illicium verum (star anise)
- •4.4.10 Syzygium aromaticum (clove)
- •4.4.11 Juniperus sabina (savin juniper)
- •4.4.12 Pimpinella anisum (anise)
- •4.4.13 Lavandula stoechas (French lavender)
- •4.4.14 Artemisia vulgaris (mugwort)
- •4.4.15 Melaleuca alternifolia (tea tree)
- •4.4.16 Pelargonium graveolens (rose geranium)
- •4.5 Safe use and precautions
- •4.5.1 Safety guidelines and precautions
- •4.6 Conclusions
- •References
- •5.1 Introduction
- •5.2 Effect of drought or water deficiency on the morphology of medicinal plants
- •5.4 Effect of drought or water deficiency on secondary metabolites of medicinal plants
- •5.5 Different approaches to mitigate the negative effects of drought stress on plants
- •5.6 Case studies
- •5.7 Conclusions
- •References
- •6.1 Introduction
- •6.2 Importance of medicinal and aromatic plants
- •6.3 Salinity effect on medicinal plants
- •6.3.1 Effects on growth and development
- •6.3.2 Impact on photosynthesis and water relations
- •6.3.3 Ionic stress and nutrient imbalance
- •6.3.4 Oxidative stress and antioxidant response
- •6.3.5 Impact on secondary metabolite production
- •6.4 Molecular responses to salinity stress
- •6.5.1 Amino acids
- •6.5.2 Proteins
- •6.5.3 Carbohydrates
- •6.5.4 Lipids
- •6.6 Study of alkaloids through proteomic and other approaches
- •6.7 Phenolic compounds during stress
- •6.8 Strategies for improving salt tolerance in MAPs
- •6.8.1 Exogenous application of plant growth regulators
- •6.8.2 Use of beneficial microorganisms
- •6.8.3 Genetic approaches
- •6.8.4 CRISPR/Cas9 gene editing
- •6.8.5 Agronomic practices
- •6.8.6 Use of mulches
- •6.8.7 Application of organic amendments
- •6.8.8 Silicon supplementation
- •6.8.9 Application of polyamines
- •6.8.10 Nanofertilizers and nanoparticles
- •6.8.11 Application of melatonin
- •6.9.1 Water relations and osmotic adjustment
- •6.9.2 Ion homeostasis and nutrient balance
- •6.10 Molecular mechanisms of salt tolerance
- •6.11.1 Genetic engineering strategies
- •6.11.2 Identification of salt-tolerant genes
- •6.11.3 Use of plant growth regulators
- •6.12 Conclusion and key points
- •References
- •7.1 Introduction
- •7.2 Heavy metals and their effects on the environment
- •7.4 Processes of heavy metal uptake by roots
- •7.5 Transport and accumulation in various plant tissues
- •7.8 Plant defense mechanisms against heavy metals
- •7.9 Molecular and genetic responses to heavy metal contamination
- •7.11 Selection of heavy metal-resistant plants
- •7.12 Case studies
- •7.13 Conclusions
- •References
- •8.1 Introduction
- •8.2 Metabolic and hormonal responses to abiotic stress
- •8.3 Water stress
- •8.3.1 Drought stress
- •8.3.2 Waterlogging stress
- •8.4 Temperature stress
- •8.4.1 High temperature (heat shock)
- •8.4.2 Low-temperature stress
- •8.5 Light stress
- •8.6 Salt stress
- •8.7 Nutrient stress
- •8.8 Heavy metal stress
- •8.9 Molecular docking calculation for stress
- •8.10 Conclusion
- •References
- •Part III: Pharmaceutical use of medicinal plants
- •9.1 Introduction
- •9.2 General properties of medicinal and aromatic plants used in burn treatment
- •9.2.1 Phytochemical content and mechanisms of action
- •9.2.2 Antimicrobial effects
- •9.2.3 Wound-healing effects
- •9.2.4 Analgesic effects
- •9.2.5 Advantages and disadvantages of herbal treatments
- •9.2.5.1 Advantages
- •9.2.5.2 Disadvantages
- •9.3 Medicinal and aromatic plants used in burn treatment
- •9.3.1 Aloe vera
- •9.3.1.1 Clinical effects
- •9.3.2 Calendula officinalis (Calendula)
- •9.3.3 Centella asiatica (gotu kola)
- •9.4 Molecular basis of plant action mechanisms
- •9.4.1 Cellular mechanisms in wound healing
- •9.4.2 Innovative research methods in herbal treatments
- •9.4.2.1 Omic technologies: genomic, proteomic, and metabolomic approaches
- •9.5 Formulation and application methods of herbal products
- •9.5.1 Pharmaceutical formulations
- •9.5.2 Dosage and application methods
- •9.5.3 Nanotechnological approaches
- •9.5.4 Factors affecting chemical stability
- •9.5.4.1 Stability enhancement methods
- •9.5.4.2 Importance of storage conditions
- •9.5.4.3 Stability tests and quality control
- •9.6 Clinical research and evidence-based practices
- •9.6.1 Clinical studies
- •9.6.2.1 Meta-analyses and literature reviews
- •9.7 Safety and side effects
- •9.7.1 Toxicological risks
- •9.7.2 Side effects and contraindications
- •9.8 Integration of traditional knowledge and modern science
- •9.8.1 Ethnobotany and traditional knowledge
- •9.8.2 Cultural and regional diversity
- •9.9 Future research areas and innovation
- •9.9.1 Pharmacogenetics and personalized medicine
- •9.9.2 Biodegradable and smart materials
- •9.9.3 Combined use of herbal treatments
- •9.10 Conclusion
- •References
- •10.1 Introduction
- •10.2 COPD
- •10.3 Asthma
- •10.4 Pneumonia
- •10.5 Lung cancer
- •References
- •11.1 Introduction
- •11.2 Oxidative stress
- •11.2.1 Reactive oxygen species
- •11.2.2 Sources and generation of free radicals
- •11.3.1 Lipid peroxidation
- •11.3.2 Protein oxidation
- •11.3.3 DNA oxidation
- •11.4 Defense of the organism against ROS
- •11.4.1 Free radicals and antioxidants
- •11.4.2 Antioxidants action mechanism
- •11.5 Methods for determination of antioxidative activity
- •11.5.1 Methods based on hydrogen atom transfer
- •11.5.2 Methods based on electron transfer
- •11.5.3 Other methods for determination of antioxidant potential
- •11.6 Medicinal and aromatic plants as natural antioxidants
- •11.7 MAPs with antioxidant activity
- •11.8 Conclusion
- •References
- •12.1 Introduction
- •12.2 Definition, historical documents, and distribution related to the study of the usage of MAPs
- •12.3 Antibacterial activity of MAPs
- •12.4 Extracts and essential oils from MAPs as antibacterial agents
- •12.5 Compounds of essential oils with antibacterial properties and their activity against a variety of bacterial strains
- •12.6.2 Terpenoids from MAPs as antibacterial agents
- •12.6.3 Alkaloids from MAPs as antibacterial agents
- •12.7.2 Clinopodium nepeta (L). Kuntze
- •12.7.3 Lavandula officinalis
- •12.7.4 Helichrysum italicum
- •12.7.5 Mentha piperita
- •12.8 Conclusion
- •References
- •13.1 Introduction
- •13.2 Medicinal and aromatic plant-derived extracts
- •13.2.1 Extraction techniques of MAPs
- •13.2.2 Influence of extraction operational parameters
- •13.3 MAPs in skin care products
- •13.3.1 MAPs as photoprotective agents against UV light and skin damage
- •13.3.2 Regenerative and wound-healing properties of MAP-derived agents
- •13.3.3 MAPs as skin anti-aging and whitening agents
- •13.4 MAPs in hair cosmetics
- •13.4.1 MAPs in hair products
- •13.4.2 MAPs in hair growth products
- •13.5 MAPs in oral hygiene products
- •13.5.1 Formulations for toothpaste and mouthwash
- •13.5.2 MAPs in prevention of dental caries
- •13.6 MAPs enhanced by sustainable materials in cosmetics
- •13.6.1 Nanotechnology in cosmetic formulations
- •13.6.2 Innovative nanocarrier materials
- •13.7 Conclusion
- •Abbreviations
- •References
- •14.1 Introduction

Chapter 13 Medicinal and aromatic plants used in cosmetics 463
and TFC of 25.79 mg RE/g db. The best MAE parameters were 26 mL/g of LSR and 606 W
for 2 min to enable TPC and TFC recovery of 17.74 mg GAE/g db and 8.11 mg RE/g db,
respectively. Similarly, 12 natural deep eutectic solvents were produced for recovering
phenolics and terpenoids from Abelmoschus sagittifolius (Kurz) Merr roots; citric acid/
glucose and lactic acid/glucose, with a molar ratio of 2:1 were the most suitable. For the
highest terpenoid recovery at 69 ± 2 mg UA/g dw, the following conditions of UAE were
used: 40 mL/g liquid-to-solid ratio, 40% water content, 30 °C, and 600 W ultrasonic
power for 5 min. Regarding phenolics recovery, 150 W ultrasonic power was the most
suitable at 9.56 ± 0.17 mg GAE/g dw. The conditions for MAE were 50 mL/g liquid-to-solid
ratio, 20% water content, and 400 W microwave power for 2 min to achieve the maximum phenolics and terpenoids at 22.13 ± 0.75 mg GAE/g dw and 90 ± 1 mg UA/g dw, respectively [14].
13.3 MAPs in skin care products
13.3.1 MAPs as photoprotective agents against UV light and skin damage
Skin is often exposed to UV radiation and produced ROS is mainly responsible for oxidative damage and accumulation of oxidative products that leads to expression of elastase
and collagenase. Moreover, skin aging is influenced by UV light and oxidative stress,
which cause acute inflammatory reactions in the tissue. Numerous natural metabolites
are strong antioxidants and show anti-inflammatory responses helpful in photoaging
condition [
ascena oil nanoemulsion at 50 mg/g and 100 mg/g emulgel doses to investigate protective
impact against UVB-influenced photoaging, measured antioxidant, antiwrinkle, and antiinflammation parameters (CAT and SOD; MMP-9; TNF-α, and IL-6), etc. Moreover, total
RNA isolated from rat dissected joints was used to evaluate the genes expression (JNK,
ERK1/2, and p38 MAPK). Given results showed that R. damascena oil nanoemulsion
achieved more significant antiaging potency versus R. damascena emulgel according to
histological and biochemical evaluations. Such extraordinary activities might be linked
with its chemical composition, geraniol, nerol, citronellol, phenyl ethyl alcohol, and linalool (29.2%, 23.4%, 16.34%, 4.96%, and 3.24%, respectively).
potentials. Five pigments of anthocyanins were characterized from methanolic extracts
and their potential to protect human dermal fibroblasts against UV-A radiation was evaluated by MTT cell growth assay and Comet assay. These extracts showed high photoprotective activity in fibroblasts emphasizing their ability to protect skin against the UV-A
radiation negative effect [17]. Non-phototoxic chamazulene as major compound (38.92%)
of Artemisia sieversiana Ehrhart ex Willd. EO in synergy with two UVB filters (ratio of
15]. Abdallah et al. [16] prepared R. damascena emulgel (100 mg/g) and R. dam-
Strawberry (Fragaria × ananassa) rich in anthocyanins has strong anti-inflammatory

464 Emina Boškailo et al.
./s-
--
--
--
Medcial benefit Reference
profile
Yield (%) Phytochemical
Extraction
parameters
(plant:
solvent)
Extraction Solvent Ratio
Acne treatment,
fragnance in
perfumes
Flavonoids, phenolic
molecules, aromatic
compounds,
. g,
.%;
. g,
extract, then exposed to
second chloroform and
g: mL First hexane crude
chloroform,
and methanol
saponins, tannins,
iridoids, and
quinones
.%;
. g,
.%
third extraction.
Wound healing ./s-
Terpenes, phenolics,
and alkaloids
. g,
. g,
extracted with mL
– g of powdered leaves
hexane, and
. g
solvents at °C, °C,
water
and °C, h. After
that, viscous semisolid
masses were evaporated.
Wound healing ./s-
Alkaloids, flavonoids,
steroids, and tannins
., .,
.,
.. g
several solvents for – h
and evaporated.
– Soxhlet extraction with
acetone,
chloroform,
methanol and
water
Table 13.1: Different extracts of medicinal and aromatic plants (MAPs) obtained using conventional and innovative extraction techniques along with operational
parameters aimed at achieving MAP phytochemical profile and getting insight to discover potential natural metabolites that may provide versatile medicinal
activities.
type
Origin Mass Grounding
organ
Plant species Plant
Thymus vulgaris Herb Wild g Powder SE Hexane,
Leaves Wild g Powder SE Methanol,
Ajuga integrifolia
Buch.-Ham
Leaves Wild – Powder SE Hexane,
Murraya
paniculata

Chapter 13 Medicinal and aromatic plants used in cosmetics 465
./s-
--
Anti-cancer, anti-
microbial, anti-
Flavonoids, phenolic
lignans and stilbenes;
Agitating:
min, rpm, RT.
O,
MeOH:
H
diabetes, and
gastrointestinal
diseases; tremors,
Rutin, psoralen,
limonene, and
pinene; oleuropein;
:, v/v
paralysis, nervous
disorders;
cardioprotective
pigenin, coumarins,
myristicin; phenolic
acid, flavonoids,
activity; cyto-, gastro-,
brain-, nephron-
tannins, amino acids,
and alkaloidal
protective effects;
[7]
Aromatherapy,
headaches,
depression, and colds
(α-terpinolene and (–)
borneol), phenolic
– Terpenoids
exposed do Clevenger-
type HD; g in mL
water exposed to
microwave digestion
(, W): temp.
increased to °C in
min and maintained
./s-
Anti-aging,
– Trans-
for min.
--
hyperpigmentation,
and acne treatment
Cinnamaldehyde
the frequency set at
kHz, the temperature
set at °C
(continued)
methanolic
mg Powder Agitating Hydro-
Botanical
growing
Leaves;
leaves
Salvia officinalis
L., Rosmarinus
solution
and
young
officinalis L., and
Mentha piperita
stems
L.; Ruta
graveolens L.,
Olea europaea L.,
Petroselinum
crispum Mill.,
Punica granutum
L.
Water – g in mL water
HD and
microwave-
particle
Flowers Field g Sieved to a
L.
Lavandula
angustifolia
assisted
hydrodistillation
(MHD)
size
between
and
mesh
Ultrasonic Methanol – the power set at W,
powderd
at particle
– Sieved and
growing
Leaves Botanical
Cinnamomum
cassia
size of mesh

466 Emina Boškailo et al.
./s-
--x
--
Medcial benefit Reference
profile
Yield (%) Phytochemical
Extraction
parameters
(plant:
solvent)
Extraction Solvent Ratio
Anti-aging and
anti-cancer
triterpenes,
sesquiterpenes,
– Flavonoids,
Extraction time (, ,
, , and min),
extraction temperature
: (mL:
g)
%)
phenolic acids,
(, , and °C),
sterols, and
coumarins
and/or the ratio of liquid
to material (, , ,
and : (v/w) mL/g) and
ethanol concentration
(%, %, %, %, and
% (v/w))
Alopecia treatment ./s-
phenolic acids
derivatives, alkaloids,
and flavonoids
g Glucosinolates,
at room temp. with
frequent shaking for h.
The soaked seeds were
cold pressed, filtered, and
seeds
soaked in
water
Water kg
Cold pressed,
filtration,
lyophilization
the filtrate was
( × L)
centrifuged at , rpm
for min. The
supernatant was
separated in a gel form
and lyophilized. After
h. a lyophilized dry
powder was produced
( g).
Origin Mass Grounding
Table 13.1 (continued)
Plant species Plant
type
organ
Wild kg Crushed SE Ethanol (conc.
Herb
(leaf,
stem,
Taraxacum
mongolicum
Hand.-Mazz
and
ground
root)
Lepidium sativum Seed Market kg Coarse

./s-
-w
Antioxidant and skin
anticancer properties
Flavonoids, tannins,
terpenoids, saponins,
g
(%) and
alkaloids, steroids,
and cardiac
g
(%)
glycosides
Chapter 13 Medicinal and aromatic plants used in cosmetics 467
[8]
Antimicrobial,
antioxidant, and
wound headlining
Phenol, ,-bis
(dimethyl ethyl),
benzene dicarboxylic
acid, squalene;
pentanoic acid, -
hydroxy-,,-dibutyl
phenyl ester, phytol,
tetramethyl
heptadecane,
neophytadiene, and
hexadecanal
.
(.%)
and .
(.%)
g/ g
sample in deionized water
at °C for h, with
– Decoction: g of
Aqueous and
hydroalcoholic
extracts
maceration
Wild g Powder Decoction and
parts
Calotropis procera Aerial
continuous stirring at
, RPM. Hydro-
alcoholic extract: g
macerated in % ethanol
(. L).
Pressure ( bar) and
–
P. juliflora Leaves Wild Powder SFE and SE Ethanol and
temperature ( °C)
g of
hexane
dynamic extraction time
the
( min).
P. julifora
leaf
powder
in
mL
hexane

468 Emina Boškailo et al.
5:1) incorporated into sunscreen formulations reduces the usage of UVB filters up to
66%. Moreover, both have ability to minimize UVB-induced radiation cellular damage,
which implies their possible application in the sunscreen products [18]. Also, the photoprotective effect of phenolics (oxyresveratrol and kuwanon O), obtained from the Morus
australis (root) extract, in human primary epidermal keratinocytes was evaluated. Both
phenolics were nontoxic to cells (conc. >10 and 0.5 μM). Oxyresveratrol increased cell viability at pretreatment at conc. 5 and 10 μM and attacked UVA- or H
-induced cellular
2O2
ROS and also reduced UVA-improved nitrotyrosine. Kuwanon O also presented similar
results with 0.25 μM and 0.5 μM, but without protection on cell survival after UVA irradi
ation. Both natural metabolites might be ingredients in cosmetic products aimed for skin
photoprotection or the prevention of photocarcinogenesis in humans [19].
13.3.2 Regenerative and wound-healing properties of MAP-derived agents
Wound represents the disruption of the cellular and anatomic tissue layer due to several types of traumas (physical, thermal, microbial, etc.) or caused by immunological
trauma. Accordingly, wound healing is a complicated process followed by repairing
damaged tissue and depends on different phases such as inflammatory, proliferative,
or remodeling. The final goal of wound healing is to reduce healing duration and mini
mize consequences such as scars. The healing process is dependent on physiological
mechanisms like anti-inflammatory, antioxidant, and antimicrobial activities. Infected
wounds are the main reason for wound-healing complications influencing efficiency of
wound healing. It is well-known that bacteria are directly linked to infected wounds, so
minimizing their load would be beneficial in the healing process. Many MAPs promote
the skin’s natural recovery processes and show potential in wound treatment. The employment of MAP extracts in wound care is constantly increasing thanks to their wide
spectra of compounds and physiological and pharmacological efficiency [20].
Numerous in vitro and in vivo methods might be employed in analyzing woundhealing performances of MAPs metabolites (Figure 13.1). In vivo artificial and tissue
models, and others might be used according to factors taken into consideration. In vitro
models are more robust, fast, and require less ethical considerations, and give detailed
insight into biochemical and physiological processes that are influenced by the test
agent/compound. It is important to emphasize that no animal tissue is an exact replica
of human skin. Cream products based on Kalanchoe pinnata (KP leaves) extracts contain
0.15% of [quercetin 3-O-αused to investigate a rat excision model for 15 days, and on the 12th day, rat groups were
treated with KP leaf-extract and its major flavonoid. The results have shown 95.3 ± 1.2%
and 97.5 ± 0.8% of healing, respectively with significant re-epithelialization and denser
collagen fibers that have huge importance in wound healing [21]. Gel formulated from
B. pinnatum (leaves) aqueous extract (5%) was evaluated for treatment of back skin
L-arabinopyranosyl-(1→2)- α-L-rhamnopyranoside]. Creams are
-
-

Figure 13.1: The proposed comprehensive scheme of several classes of human models of wound repair
such as in silico, in vitro, ex vivo, in vivo, as well as applicable assays for various wound models [23].
Chapter 13 Medicinal and aromatic plants used in cosmetics 469
wounds in rats. The wounds reduction was followed by a reduction in inflammatory infiltrate and the levels of the IL-1β and TNF-α. The formulated gel exhibited phytochemical
and biological stability for a month and showed quercetin 3-O-α-
-(1→2)-O-α-
L-rhamnopyranoside (B. pinnatum compound) as significant chemical marker
L-arabinopyranosyl
of MAP extracts and formulations containing B. pinnatum that might be used in evaluation of quality [22].
13.3.3 MAPs as skin anti-aging and whitening agents
Today’s skin care is very complex, and women in early ages (from 30 years) are showing signs of aging skin. The processes on skin are the most noticeable; the level of skin

470 Emina Boškailo et al.
care products is highly in demand. The most age-related changes in the dermis include: (a) a decrease in the number and activity of fibroblasts, that are important in
producing collagen, hyaluronic acid, and elastin, (b) breakdown of collagen fibers, increased cross-linking, and a decrease in skin resilience and stretchability, (c) alterations in elastin fibers, leading to clumping (elastosis), no elasticity, and wrinkle formation, and (d) a reduction in hyaluronic acid, resulting in skin that is less moisturized
and less resilient. Botanical ingredients are commonly used in cosmetic products for
dry and mature skin due to their ability to enhance hydration status of skin, decrease
trans-epidermal water loss, strengthen the skin barrier, and prevent the breakdown
of skin components. Plant extracts and natural products are valued for maintaining
skin integrity and structure, offering promising anti-aging benefits. In vitro studies
have demonstrated that MAPs might be a beneficial source of agents with huge potential anti-aging performances [24].
A systematic molecular modeling study explored the anti-aging effects of Ros-
marinus officinalis L. hexane extract (RHE) by analyzing the inhibitory impact of its
major components on key aging-related enzymes, including elastase, collagenase,
and hyaluronidase. The RHE was incorporated into lipid nanocapsule-based mucoadhesive gels (particle sizes from 56.55 nm to 66.13 nm), uniform distribution (PDI
0.207–0.249), and negative zeta potential (−13.4 to − 15.6). In an in vivo UVB-irradiated
rat model, the RHE-loaded gel provided photoprotection, improved antioxidant levels, enhanced epidermal and dermal histology, and reduced inflammation and wrinkle markers. Moreover, in silico molecular modeling identified verbenone, crucial
for RHE anti-elastase activity, due to high docking score and favorable binding mode
(Figure 13.2) that might be responsible for in inhibiting elastase, an enzyme involved
in skin aging [4].
Skin whitening or lightening is mainly connected to practice in some ethnic groups
for culture-specific beauty preferences by decreasing human melanin concentration or
applying some plant-based or synthetic substances to change the skin tone or lighten it.
Whitening is often referred to dermatological conditions, for treatment hyperpigmentation, or post-inflammatory hyperpigmentation, or conditions such as vitiligo when the
skin loses pigment or its function is disabled [25]. A natural cosmetic product consisting
of Hibiscus cannabinus L. extract was developed and evaluated on antioxidant, antityrosinase, and anti-aging activities. The results have shown antityrosinase potential on inhibition of monophenolase (30.28 ± 3.90%) and diphenolase (11.40 ± 0.29%) formation, and provided inhibition of collagenase (36.41 ± 0.54%) and elastase (23.13 ± 1.56%) [26]. Several
MAPS and their aqueous extracts were exposed to the anti-aging activities, Echinacea pur-
purea J. Presl has shown the best inhibition of collagenase, elastase, and hyaluronidase
activity (78.5 ± 0.0, 69.0 ± 1.4, and 64.2 ± 0.3%). Also, Morus alba L. (leaves and steamed/
roasted leaves) revealed the best anti-inflammatory potential, as they inhibited IL-6 and
TNF-α secretion (p < 0.05). These aqueous extracts pose significant impacts on the skin

Figure 13.2: The representation of verbenone in the docking pose in elastase: (a, b) verbenone in 3D
docking pose and 2D interaction diagram of in the binding site of elastase, (c, d) collagenase, and (e, f)
hyaluronidase. Reproduced with permission from [4]. Copyright Nature ©2022.
Chapter 13 Medicinal and aromatic plants used in cosmetics 471
and might be applied in cosmetic formulations like toners, facial mist, and facial serum
[27]. A comprehensive summary of MAP extracts and their major constituents are given
in Table 13.2, investigated by various in vitro, in vivo, and in silico methods applied in
evaluation of their potential for cosmetic skin care formulations.

472 Emina Boškailo et al.
Inhibition (%) Reference
viability
(%)
IC Cell
Human
cells
area
. and g/mL – [28]
Wound healing HDF,
HaCaT
– [29]
– At
conc. g/
mL >
HUVEC
[30]
At conc. g/mL:
Tyrosinase:. ± .
From . to
.%
Reduced the
migration of Ca-
Ca-
oral
Skin aging,
wound healing,
(seeds) and . ± .
(pulp); Hyaluronidase:
. ± . (seeds)
cells from .% to
%
carcinoma
cells
- cells
proliferation of
Ca
[31]
> and ; Elastase:
MeOh up to
HaCaT, BJ – – Collagenase: MeOH
Anti-aging
properties
Skin whitening – – – ., DPPH of . [32]
Table 13.2: Medicinal and aromatic plant extracts with their major constituents in maintaining skin care with huge benefits for skin aging, wound healing, and skin
whitening.
Model Assay Application
compound
Plant Extract Active
assay test
In vitro Cytotoxicity and scratch
Asiaticoside
(MF of .%)
: w/v)
EtOH
(
%
Centella
asiatica
In vitro Scratch assay test Wound healing HDF,
–, (– g/
mL)
Aqueous
extrac
Crocus sativus
L.
assay, clonogenic assay
In vitro Trypan blue cytotoxicity
, g/mL
MeOH –, –
Solanum
betaceum
denaturation;
determination of anti-
In vitro Inhibition of protein
–, –,
g/mL
MeOh
and
MeOh-
Borago
officinalis
collagenase and anti-
Aq
elastase activity
Aq –, , g/mL In vitro Inhibition of tyrosinase
Myracrodruon
enzyme, antioxidant
activity
urundeuva
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