Dragon Fruit (Hylocereus undatus)Peel: Powerful
Source of Nutrition and Health
Hiten
Khattar, Shabnam Ain*1, Qurratul Ain1, Himani Bansal1,
Mohd Uzair1, Chhaya
Rathore Sahu2, Ajeet1, Al Alexis Ain1 & Cutee1
1. Sanskar College of Pharmacy and Research, Ghaziabad, Uttar
Pradesh
2. Rajiv Gandhi College of Pharmacy, Nautanwa, Maharajganj, Uttar
Pradesh
*Correspondence: shabnam.ain@sanskar.org;
DOI: https://doi.org/10.71431/IJRPAS.2026.5404
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Article
Information
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Abstract
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Review Article
Received: 24/04/2026
Accepted: 27/04/2026
Published:30/04/2026
Keywords
Antioxidant Activity; Betalains;
Dietary Fibre;
Dragon Fruit Peel (Hylocereus spp.); Phenolic
Compounds
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The fruit of the dragon fruit (Hylocereus
undatus) is famous not only for its external appearance but also for its
nutritional value. The peel of dragon fruit is approximately 20-40 per cent
of the weight and is normally treated as agricultural waste; however, it
possesses some hidden nutritional value and is very valuable. The main
message of this review is that dragon fruit peel should be used because it is
both nutritionally and therapeutically significant, as well as economical. It
also aims to identify the major chemical compounds found in the peel and
their applications in promoting health. This review also summarizes the data
of recent analytical studies where standard tools were used, including
solvent extraction and HPLC, followed by chromatographic and spectroscopic
methods for the identification and quantification of chemical compounds found
in the peel. The analysis established that the peel of dragon fruit majorly
harbors three bioactive agents: betalains, phenolic compounds, and dietary fibres.
They all contain unique therapeutic properties, such as betalains, which
possess strong antioxidant properties and also provide the fruit with colour;
phenolic compounds, which possess antimicrobial properties; and dietary fibres,
which regulate blood sugar levels and improve gut health. It has been proven
that the peel of the dragon fruit is not a waste, but a powerful source of
health-promoting compounds that would help to reduce the effects of pollution
on the environment and foster the economic and nutritional industries.
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INTRODUCTION
Pitaya, also known as strawberry pear or dragon fruit, is a unique
cactus fruit. This fruit is native to Central and South America [2]. This fruit
is very popular because of its striking colours and various
health benefits. The fruit is beneficial, and its peel also contains
various nutritional characteristics. It is a red or pink-skinned fruit covered
with scales, with white or red flesh and small black seeds [2]. The taste of
dragon fruit is mildly sweet, but it is rich in vitamin C and has antioxidant
properties [2]. It has a high fibre and low-calorie content, making it suitable
for fruit consumption during weight loss. This fruit is native to Mexico and
North America but now is cultivated nearly everywhere on earth, with the
highest production in Southeast Asia and other tropical and subtropical regions
[2].
Dragon fruit peel is often regarded as waste and discarded, which may
further contribute to the production of harmful greenhouse gases and damage the
soil, thereby providing favourable conditions for bacterial growth and the
development of harmful diseases [1]. Countries such as Vietnam, which lead in
dragon fruit production, produce over a million metric tons of dragon fruit
peel waste annually and discard approximately 220,000 tons of peels [6].
Researchers can use this waste produced by dragon fruit peels because it is
rich in valuable compounds that offer several health benefits, and because the
demand for such organic products grows daily because of their effectiveness and
low side effects [1]. The extraction of bioactive materials yields economic
benefits.
The dragon fruit peel contributes to almost 22-44% of the fruit weight [1].
The main compounds found in dragon fruit peel are betalains, anthocyanins,
flavonoids, phenolic compounds, pectin, and dietary fibre, which are known for
their antioxidant, anti-inflammatory, antimicrobial, and anticancer properties [3].
This review article focuses on the chemical components of dragon fruit peel,
their important functions and uses, and future research directions on the peel.
Botanical information
There are many species of
Dragon Fruit based on their flesh and skin. Among all pink peel dragon fruit,
the most common is the one containing white flesh. Dragon fruit is often
referred to as pitaya. It was once called the genus Hylocereus, but recent phylogenetic
research has transferred these species to the genus Selenicereus. The table 1 shows the botanical info for the
different dragon fruit species.
Table 1: Different
dragon fruit species with their descriptive features
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Common Name
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Botanical Name
|
Family
|
Distinctive Features
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|
White
Pitaya
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Selenicereus
Undatus
|
Cactaceae
|
Bright
Pink Peel, Mild White Flesh
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|
Red
Pitaya
|
Selenicereus
Polyrhizus
|
Cactaceae
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Pink Peel, Vibrant
Magenta Flesh
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Yellow
Pitaya
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Selenicereus
Megalanthus
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Cactaceae
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Yellow thorny peel with white flesh
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Taxonomy of dragon fruit
o
Kingdom: Plantae
o
Division: Spermatophyta
o
Class: Dicotyledonae
o
Family: Cactaceae
o
Genus: Selenicereus (Formerly –
Hylocereus)
o
Species: Selenicereus
Udantus, Selenicereus Costaricensis,
Selenicereus Megalanthus
Figure 1: Different species of dragon
fruit
Plant description
Catia or dragon fruit is a cactus plant that belongs to the cactus
family (Cactaceae). Dragon fruit, being a climbing or aerial plant, requires
support from another plant or object to grow. The Primary stem of the plant is
dense and moist and exhibiting a triangular geometry. As a cactus species, the
dragon fruit stem holds up the essential nutrients and water needed by the
plant to grow in harsh or extreme weather, such as low humidity and infertile
soil. The flowers of the plant are deep greenish yellow or pale white in colour
and have an aromatic smell. The length of the flower is approximately 20-35 cm,
and its thickness is approximately 22-35 [4].
PEEL OF DRAGON FRUIT
Dragon
fruit contains various compounds, such as betalains, pectin, phenolic compounds,
flavonoids, and dietary fibres. The compounds have their own functions, such as
betalains and anthocyanins, which are responsible for the antioxidant
properties and the red colour of the fruit; pectin and dietary fibres are
responsible for treating gut health and texture of the fruit; phenolic
compounds and flavonoids are responsible for the anti-inflammatory and
antimicrobial effects; and various polysaccharides are also responsible for the
antioxidant properties and metabolic regulation in the body [5].
Betalains (betacyanins)
Betalains
are tyrosine-derived pigments mainly found in plants of the genus
Caryophyllales. Betalains are water-soluble, similar to anthocyanins, and are
found in vacuoles of plant cells. Betalains are water-soluble, like anthocyanins,
and exist in vacuoles. The word betalains is derived from the Latin name of
beetroot, that is Beta Vulgaris,
through which the Betalains were extracted for the first time. Betalains is
responsible for the reddish-pink colour of the fruit or flowers of plants.
Basically, the Betalains are classified into two categories [7] i.e.
Betacyanins and Betaxanthins. The colour of dragon fruit is
primarily due to betalains, which are also natural colouring agents in the food
industry. Betalains are closely related to anthocyanins, except that they are
not found in all angiosperms but only in subdivisions of Caryophytes and in
isolated genera of Basidiomycota.
Dragon fruit is regarded as the third richest source of Betalains after the Beta vulgaris and Amaranthus species. In dragon fruit, the two categories of
betalains have their own characteristics, as betacyanins are responsible for
the red-violet colour. In contrast, the betaxanthins are responsible for the
yellow-orange colour [1]. It has been found that betalain content is higher in
the peel than in the pulp; hence, the peel, or waste, has more betalain content
than the original fruit. Table 2 shows the betalain content of various
dragon fruit species reported in the literature. Based on these observations,
it can be concluded that the betalain content is higher in dragon fruit than in
Beta vulgaris [1].
Table 2: Betalain (betacyanins) content in different dragon fruit
species.
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Species
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Betacyanin Content
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Material
|
Extraction Method
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H. polyrhizus
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7 mg / 100 g dm
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Fresh Peel
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Methanol, 1:4 (g
mL−1), 24 h
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H. polyrhizus
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197 mg/ 100 g dm
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Fresh Peel
|
Chilled 80% acetone solution, 1:4 (g g
-1) and 10 and 5 min respectively.
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|
H. polyrhizus
|
1046 mg/ 100 g
dm
|
Fresh Peel
|
Ethanol 60%,
1:3.57 (g mL−1), 12 h, 3 times
|
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H. polyrhizus
|
97 mg/ 100 g dm
|
Air Dried Peel
|
Oven drying: 42 °C for 24 h
Extraction: ethanol 50%, 1:1 (g mL−1), 20 min
|
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H. polyrhizus
|
8021 mg/ 100 g
dm
|
Fresh Peel
|
Water, 1:25 (g g−1)
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4155 mg/ 100 g dm
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Drum Dried Peel
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Drum drying: 1 rpm, 2 bar, 0.1 mm gap,
5–10 min
Extraction: water, 1:25 (g g−1)
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H. polyrhizus
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377 mg/ 100 g dm
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Freeze-Dried
Peel
|
Freeze drying:
4.6 Pa, −54 °C, 72 h to 25 °C
Extraction: water
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H. undatus
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197 mg/ 100 g dm
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Freeze-Dried Peel
|
Freeze drying: 4.6 Pa, −54 °C, 72 h to
25 °C
Extraction: water
|
The betalain content of H. polyrhizus and H. undatus was similar. They
contain various compounds like betanin, phyllocactin, isobetanin and
isophyllocactin, whereas in the Beta vulgaris, in which betanin and isobetanin
are found in abundance [1].
The chemistry of betalains can be understood as Betalains were first
isolated and their chemical structures were discovered in 1960 by Dr. Tom Mabry
at the University of Zurich. Betalains and anthocyanins are similar but
chemically and structurally different and cannot be discovered in a single
plant. Betalains contain nitrogen in their structure, whereas anthocyanins do
not contain the nitrogen [7]. Tyrosine serves as the precursor for the
betalains which are indole derivatives. The most common betalains are betanin,
a glucoside that yields glucose and betanidin upon hydrolysis [7]. Betalains
are pigments containing a nitrogen molecule and have a core structure of
betalamic acid. The liquefication of betalamic acid with cyclo-DOPA results in
the formation of betacyanins, and condensation with amino acids and their
derivatives leads to the formation of the second category of betalains,
betaxanthins. Until 1957, betalains were considered nitrogenous anthocyanins;
however, their crystallization, hydrolysis, and other reactions demonstrated
that they are distinct [8].
Biosynthesis of betalains: There are two
enzymes responsible for the biosynthesis of betalains: bifunctional cytochrome
P450 enzymes CYP76AD1, and (2) 4,5- DOPA dioxygenase (DODA). In the first step,
tyrosine is hydroxylated to L-DOPA by CYP76AD1. In the second step, the
cyclization of DODA takes place. Betalamic acid condenses with cyclo-DOPA and
amine, cyclo-DOPA’s glucosyl derivatives, forming betacyanins and betaxanthins [9].
Figure 2: Biosynthesis
of betalains
Extraction process and uses of
betalains: Betalain extraction can be carried out in either pre-cooled water,
aqueous methanol, or methanol at a pH of 5, with 0.25% (w/v) ascorbic acid to
improve stability because of their hydrophilic nature. The extracts are
processed by precipitating the pectic substance and using ion-exchange
chromatography to remove free sugars and organic acids [8].
Betalains have various
health-promoting benefits, including antioxidant, anti-inflammatory, and
analgesic properties. The antioxidant capacity of betalains was evaluated using
the ABTS (2,2'-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid)) assay. This
assay determines the ability of antioxidants to scavenge the free radical cat
ions ATBS. The E50 value, which determines the 50% of scavenging activity of
the betalains, was found to be 666–860 ppm. Betalains also exhibit
anti-inflammatory activity, which is assessed by their capacity to inhibit sodium
dodecyl sulfate-induced vascular irritation of the duck embryo CAM. The
anti-angiogenic properties were also evaluated by observing the formation and
depletion of blood vessels in the CAMs of duck embryos following treatment. The
betacyanins isolated from dragon fruit peel have also been shown to control
obesity. Betacyanins also reduce insulin resistance, thereby improving hepatic
steatosis in obese mice fed a high-fat diet. Antidiabetic properties are also
found in betalains, as they can increase adiponectin serum levels and reduce
FGF21 levels [7]. Betalains also exhibit antibacterial activity against both
Gram-positive and Gram-negative bacteria. The antibacterial activity of
betalains is attributed to the presence of alkaloids in their structure [1].
The betalains possess the anti-inflammatory properties and reduces the
inflammation in the stomach which ultimately reduces the formation of peptic
ulcer in the stomach thus showing the anti-ulcer property [44].
Phenolic
compounds
Pitaya fruits contain a wide range
of flavonoids and phenolic compounds, which are found in both seeds and pulp
and also in the peel (Table 3). The special characteristics of these
phenolic compounds are their possible health benefits, which are primarily
explained by their antioxidant properties [11]. Among the 57 selected studies,
pitayas of the genus Hylocereus were the most characterized fruits in terms of
the presence of phenolic compounds. The phenolic chemical profile of Hylocereus
polyrhizus has been analyzed in other studies. In the peel of H. polyrhizus,
up to 15 phenolic compounds have been identified, mainly in the flavonoid class
[18]. Epicatechin, phlorizin, and kaempferol (flavonoids) were found in the
fruit pulp. The marked presence of phenylpropanoids and flavonoids in Hylocereus
polyrhizus pitaya has been reported in other studies. Caffeic acid, along
with quercetin and its derivatives, was identified in most of the studies
involving H. polyrhizus [17].
The species Hylocereus
costaricensis has also been evaluated for the presence of phenolic
compounds [13]. Flavonoids, such as myricetin, rutoside, quercetin,
pyrocatechol, rutin, and hispidulin, were identified in the peel and pulp of
the fruits. The compounds belong mainly to the classes of benzoic acid
derivatives and hydroxycinnamic acids and their derivatives [19].
Table 3: Assay of phenolic compounds present in pitaya fruits.
|
Vegetable
Fraction
|
Fruit
|
Technique
|
Extraction Method
|
Compound
identified
|
|
Peel
|
Hylocereus undatus
|
UPLC-QTOF-MS/MS
|
Extraction
with 80% methanol, alkaline hydrolysis with NaOH solution at 60degree Celsius
+
ultrasonic bath, and finally, acid hydrolysis using ethyl acetate
|
(Benzoic
acid derivatives)
Orsellinic
acid,
(Coumarins derivatives)
Daphnetin
(Phenylpropanoids)
Sinapoyl malate.
|
|
Peel
|
Hylocereus
undatus
|
HPLC-DAD-ESI/MSn
|
Aqueous
extraction was performed in a high-performance microwave digestion unit at
600 W. Different combinations of solid/solvent ratio, temperature, and
extraction time were tested.
|
(Flavonoids)
Kaempferol,
Quercetin and Isorhamnetin derivatives
(Phenylpropanoids)
Cinnamoyl derivatives, Caffeoylquinic acid derivatives.
|
|
Peel
|
Hylocereus spp.
|
LC-MS/MS
|
Extracted by semi-continuous hydrothermal process
|
(Phenylpropanoids)
Protocatechuic, and Piperonylic acids
|
|
Peel
|
Hylocereus
lemairei
|
HPLC
|
Water
extraction under the reflux system coupled to a condenser.
|
(Flavonoids)
Kaempferol,
Quercetin and Isorhamnetin derivatives.
|
|
Peel
|
Hylocereus undatus
|
HPLC
|
Extraction with methanol.
|
(Phenylpropanoids)
p-Hydroxybenzoic,
Ellagic
Chlorogenic acids
(Flavonoids)
Catechin
|
|
Peel
|
Hylocereus
undatus
|
HPLC-DAD
|
The
powdered peel was mixed with either water or 60% ethanol and kept overnight
at room temperature (27 °C) with constant stirring (400 rpm).
|
(Phenylpropanoids)
Caffeic acid and Ferulic acid
(Flavonoids)
Quercertin
|
|
Peel
|
Hylocereus polyrhizus
|
UPLC-QTOF/MS
|
The powdered peels were mixed with 82% ethanol
|
(Phenylpropanoids)
Gallic acid,
Sinapic acid and Rutin
|
Chemical nature: Pitayas may have
different chemical and nutritional compositions depending on their origin [14].
Flavonoids such as quercetin, kaempferol, rutin, and catechin are present in
both the pulp and peel of Stenocereus species, including S. pruinosus,
S. stellatus, and S. thurberi. Although the peel of the fruits of
Hylocereus polyrhizus and Hylocereus undatus is usually discarded during
consumption, it has a huge potential in the form of bioactive phenolic
compounds related to health benefits and food use. Researchers investigated the
phenolic content of these peels by employing various extraction techniques,
including enzymatic treatment and both acid and basic hydrolysis. Typically,
phytochemical quantification focuses exclusively on free phenolic compounds,
which are easily liberated from the plant matrix [14]. Beyond standard
methanolic extraction, the researchers utilized acid and basic hydrolysis
alongside an enzymatic cocktail—comprising cellulase, hemicellulase, and
pectinase—to isolate matrix-bound phenolics. This approach revealed that bound
compounds accounted for 50% of the total phytochemicals identified in the peels
of the two studied species [15].
A total of 37 individual phenolic
compounds were characterized, spanning the chemical groups of flavonoids and
derivatives of both benzoic and hydroxycinnamic acids. Notably, the bound
fraction was dominated by caffeic, ferulic, and p-coumaric acids, whereas the
free fraction consisted mainly of chlorogenic acid, quercetin, and ferulic
acid. In addition, the identified peel phenolics were positively correlated (r
> 0.70) with the antioxidant activity (DPPH, ABTS+, and FRAP assays), this
further underscores the importance of phenolic compounds as potent natural
antioxidants.
Extraction Process: Another study
similarly utilized various extraction techniques to liberate the free phenolics
bound within the H. undatus peel matrix. Research indicates that bound
phenolic compounds possess greater biological activity than free phenolics. The
integration of ultrasound-assisted alkaline extraction proved highly effective
in maximizing polyphenol yields. The study's highlight was the identification
of daphnetin, which showed a 120-fold increase in abundance within the bound
polyphenol extract compared to the free extract [15].
Therapeutic uses: This compound
exhibits significant biological activity, demonstrating potent antioxidant,
anti-inflammatory, and anti-arthritic properties. Furthermore, it inhibits
pseudoallergic reactions and enhances cognitive function in murine models [13].
The phenolics compound serves as the natural anti-oxidant supporting the L-DOPA
lacks which help in treating Parkinson’s diseases [12]. The researchers further
noted a significant prevalence of medicarpin—a compound structurally related to
isoflavonoids—particularly within the bound polyphenol fraction [16]. This
constituent is notably linked to the prevention of postmenopausal arthritis,
inhibits osteoclast genesis, and has neuroprotective effects against
Alzheimer’s disease [25]. Flavonoids frequently identified in pitaya, including
isorhamnetin, quercetin, and kaempferol, serve as the primary active
constituents in traditional Chinese medicinal formulations used to treat
COVID-19 [20]. Flavonoids (such as quercetin and gallic acid) present in the
peel of dragon fruit contains anti-allergic properties helping in treating the
allergic reaction in respiratory tract and lungs also. The peel also contains
various anti-oxidant properties and reduces the free radical in the body which
ultimately reduces the oxidative stress which is a key factor in causing the
COPD and other lung damage. Hence promoting the lung treatment [43].
The most commonly identified
phenolic compounds in dragon fruits are described in Figure 3. The
literature indicates that phenylpropanoids are the most frequently reported
compounds, followed by those within the flavonoid class.
Figure 3. The main
phenolic compounds identified in the studies.
The findings suggest that, broadly
speaking, cactus fruits serve as excellent sources of phenolic phytochemicals.
Kaempferol and rutin are some of the main flavonoids in pitaya, and they have
been shown to have various health-promoting effects. Kaempferol demonstrates a
multifaceted pharmacological profile, encompassing antihypertensive,
cardioprotective, antioxidant, and anti-inflammatory activities [21].
It has also been found to prevent microvascular diseases caused by elevated
blood sugar levels and has the potential to alleviate liver damage caused by
alcohol [22]. Many studies have also reported Rutin. It has been found that
this compound inhibited ventilator-induced lung injury and possibly
prevents kidney injury by alleviating oxidative stress and maintaining lipid
metabolism [23,24].
Pitaya has health benefits that are
facilitated by its phenolic acid profile. Gallic acid [41] has the potential to
be naturally an inhibitor of alpha-amylase, which makes it an effective
contender that may be utilized to create functional food and nutraceuticals
that are diabetic-friendly. They show neuroprotective effects and
therapeutic effects in the management of obesity [25,26]. Ferulic acid has
various health effects. It is able to enhance glycemic metabolism, gut
protective effect through the regulation of gut microbiota and antioxidant,
hepatoprotective, and antihyperglycemic effects [27,28]. Another important
phenolic acid in pitaya is the chlorogenic acid, which also has antioxidant and
anti-inflammatory effects and enhances lipid metabolism [29]. The possible uses
in the treatment of multiple diseases can distinguish caffeic acid. It is
effective in managing cancer, diabetes, and Parkinson’s disease. Another
phenolic acid found in pitaya is protocatechuic acid, which has been shown to
have anti-diabetic effects and possible chemopreventive abilities [30].
Dietary
fibres
Dietary fibres are the nutrients
that are indigestible carbohydrates obtained from plant-based food, these do
not break down into glycon entities like other carbohydrates thus helping in
better digestion and regulating blood glucose level eventually preventing from
diabetes based on water solubility, these are generally classified as soluble
and insoluble fibres among which the fibres which are present in pitaya are
pectin and oligosaccharides and are soluble fibres [34]. They are no longer
fibres, but they form a complex in the dietary fibre due to their similar
effects [31]. Soluble dietary fibres help reduce cholesterol levels, thereby
treating conditions such as hyperlipidemia, and also have anti-inflammatory and
anticarcinogenic effects. Dietary fibres are picked out by analysis of
composition and physiological activity. These are the components that are
resistant to enzymatic digestion [32].
Chemistry: Carbon is the main
constituent of the cell walls of plants and of value to gut bacteria.
Structurally, they are complex and contain homopolygalacturonan (PG),
rhamnogalacturonan I (RGI) and rham nogalacturonan II [35]. Traditionally,
pectin is used to make jellies, jams, etc [36]. The oligosaccharides are
prebiotic, thus triggering the proliferation of the bifidobacteria and
lactobacilli. In the proximal colon, these carbohydrates are fermented by
microorganisms, yielding short-chain fatty acids, such as acetate, butyrate,
and propionate. Acetate is used in the muscles, butyrate is used for colon cell
division and has anti-colon cancer properties, and propionate is transported to
the liver for ATP synthesis [33].
Notably, in food fibre profiles,
pectin and other soluble polysaccharides are significant substances since
digestive enzymes do not digest them but affect the absorption of nutrients in
the human small intestine, and are fermented in the large intestine by
bacterial enzymes, which are useful in maintaining the colonic microflora [37].
Extraction Process: The yield ranges
from 10 to 26 g/100 g dm, which is comparable to those of other pectin sources such
as apple pomace (~25 g/100 g dm), carrots (7–19 g/100 g dm), citrus peels (~12
g/100 g dm), orange pulp (12–28 g/100 g dm), sugar beet pulp (10–30 g/100 g
dm), soy hull (~25 g/100 g dm) and sunflower (10–20 g/100 g dm)[38]. Pectin
separated using dragon fruit peels contains a wide range of degrees of
esterification, dependent on materials and processing factors, with a DE value
that can be both large (≥90 per cent) and low (<10 per cent). The pH of the
extraction medium has a strong effect on DE, whereas the effects of extraction
time and solvent-to-pectin volume ratio on pectin precipitation are moderate.
Table 4 reports the pectin yields obtained from the dragon fruit peels,
including their degrees of esterification (DE) and the conditions of extraction.
Particularly, it was found that a significant increase in pH between 2 and 3.5
led to a significant increase in DE [39]. It also had similar oil and water
holding capacities to citrus pectin. Therefore, although its viscosity
(0.088–0.1 Pa.s) at 3%w/v was lower than that of commercial apple (0.38–0.55
Pa.s) and citrus pectin (0.28–0.35 Pa.s), it displays potential as a functional
and healthy ingredient in moderately viscous foods and beverages [40].
Alternatively, the low methoxy pectin extracted from dragon fruit peels with an
esterification degree of 36% was demonstrated for their ability to be grafted
with acrylic for hydrogel formation [42]. The hydrogel had a high swelling capacity
of 3475% and was pH-sensitive, which could possibly be applied as a drug
carrier for the specific target of the colon area.
Table 4: Yields and characteristics of pectin
of dragon fruit peel.
|
Dragon
fruit species
|
Pectin
(% based on dry weight)
|
Degree
of esterification (%)
|
Extraction
condition
|
|
H. polyrhizus
|
10.8
|
N.A.
|
pH 3–4 (citric acid)
|
|
H. polyrhizus
|
15.0–20.1
|
31.1–47.0
|
Precipitation by Ammonium oxalate (0.25) and pH 4.5
(oxalic acid) and pH 1.49 (hydrochloric acid).
|
|
H. polyrhizus
|
14.9
|
~50–75
|
pH 3–4 (citric acid)
|
|
H. polyrhizus
|
10.4–16.8
|
6.5–92.1
|
pH 2–5 (citric acid)
|
|
H. polyrhizus
|
26.4
|
63.7
|
pH 2 (citric acid)
|
|
H. costaricensis
|
18.4–23.1
|
59.1–73.6
|
pH 2 (nitric acid)
|
Other than pectin, oligosaccharides
are also of great interest. Although pectin has prebiotic properties, its
effects are moderate, and pectin is generally hydrolyzed by acids, enzymes or
hydrothermal processes to obtain pectin-oligosaccharides for enhanced
biological activities [42]. Galacto-oligosaccharides (e.g. raffinose and
stachyose), malto-oligosaccharides (e.g. maltotriose to maltoheptaose) and
fructo-oligosaccharides are also other widely studied prebiotic
oligosaccharides. These kinds of oligosaccharides were detected in dragon fruit
peels of H. polyrhizus and H. undatus species (Table 5).
Dragon fruit peels seem to contain higher amounts of malto-oligosaccharides
than those of galacto-oligosaccharides and fructo-oligosaccharides. Notably,
dragon fruit peels contain significant concentrations of both raffinose and
stachyose—oligosaccharides that are absent in many other fruits and vegetables.
Therapeutic uses: The presence of
these galacto-oligosaccharides is also reflected by the significant amount of
galactose moiety detected in the dietary fibre profile of dragon fruit peels.
They have been demonstrated as important prebiotics because they can stimulate
the growth of bifidobacteria, a crucial probiotic and also one of the major
genera of bacteria that constitute the gastrointestinal tract flora in humans.
Beyond its phenolic profile, the pectin-rich matrix of H. undatus peels
offers promising anti-cancer potential. By targeting Galectin-3-mediated
pathways, pectin acts as a natural inhibitor of metastasis, complementing the
pro-apoptotic effects of daphnetin [35]. The oligosaccharides of the Raffinose
family, especially, may also serve as reserve carbohydrates, membrane stabilizers
and stress-tolerant mediators, which may help in disease prevention in humans.
Alternatively, the galacto-oligosaccharides of stachyose could improve the
composition of faecal microbes, which facilitates the intestinal peristalsis
and faecal excretion.
Table 5: Oligosaccharide
composition of dragon fruit peels (μg/100 g dm)
|
Oligosaccharides
|
Monosaccharide unit number
|
Monosaccharide unit
|
H. polyrhizus
|
H. undatus
|
|
Raffinose
|
3
|
Galactose,
glucose, and fructose
|
466
|
346
|
|
Stachyose
|
4
|
Galactose,
glucose, and fructose
|
431
|
420
|
|
Maltotriose
|
3
|
Glucose
|
407
|
207
|
|
Maltotetriose
|
4
|
Glucose
|
183
|
119
|
|
Maltopentaose
|
5
|
Glucose
|
1493
|
1354
|
|
Maltohexaose
|
6
|
Glucose
|
157
|
71
|
|
Maltoheptaose
|
7
|
Glucose
|
216
|
153
|
|
Fructo-oligosaccharides
|
2–8
|
Glucose,
fructose
|
417
|
213
|
CONCLUSION
Rather
than being dismissed as mere agricultural waste, dragon fruit peel is actually
a hidden gem with incredible potential. Making up nearly a third of the fruit’s
total weight, these peels are packed with powerful natural compounds like
betalains, phenols, and dietary fibres that offer far more than just
nutritional value. Research shows that these elements can play a major role in
fighting inflammation and managing serious health Broadening our perspective to
see the peel as a resource rather than trash could be a game-changer; it offers
a natural, eco-friendly alternative for the food and medicine industries while
helping to reduce the ecological effect left by food waste. Ultimately, what we
once threw away is proving to be a potent, health-boosting gift from nature.
CONFLICT
OF INTEREST
None.
ACKNOWLEDGEMENT
Authors would like to express their
sincere thanks to the Director of Pharmacy, Prof. (Dr.) Babita Kumar and
Management of Sanskar Educational group for their kind support.
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