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Int. J. Med. Arom.

Plants, ISSN 2249 4340


REVIEW ARTICLE
Vol. 3, No. 4, pp. 492-506, December 2013

Aloe vera L. processing and products: A review


V. K. CHANDEGARA1*, A. K. VARSHNEY2
1
Department of Processing and Food Engineering, College of Agricultural Engineering and Technology,
Junagadh Agricultural University, Junagadh 362 001 (Gujarat), India
2
Polytechnic in Agro-Processing, College of Agricultural Engineering and Technology, Junagadh Agricultur-
al University, Junagadh 362 001 (Gujarat), India
*Corresponding author: Tel: +91-0285-2671018

Article History: Received 7th November 2013, Revised 27th December 2013, Accepted 28th December 2013.

Abstract: Use of Aloe vera in nutritional, pharmaceutical and cosmetic preparations draw attention for generation of
scientific information. Looking to the importance of biologically active components possessed by the leaves of the Aloe
vera plant and its wide spread use, it has become imperative that, the leaf should be processed with the aim of retaining
essential bioactive components. In this review paper, different processing aspects like harvesting, handling, transporta-
tion, Aloe vera gel expulsion, gel extraction and storage of gel were critically described from different references. Differ-
ent product prepared from Aloe vera whole leaf and gel like food products Aloe juice, Aloe health drink, Aloe desert, etc
were reviewed. Aloe vera processing methods for gel expulsion by splitting of leaf, roller method, crushing of whole leaf,
hand filleting methods and stabilization are described with various references. Present processing techniques aims at pro-
ducing best quality aloe products but end aloe products contain very little or virtually no active ingredients. Hence, ap-
propriate processing techniques should be employed during processing in order to extend the use of Aloe vera gel.
Keywords: Aloe vera gel expulsion; Aloe vera gel expulsion extraction; filleting; leaf splitter method purification; stabi-
lization.

Introduction Aloe vera Latex (Aloin, a bitter tasting pur-


gative, is destructive to healthy tissue and cells)
Medicinal plant has specific property and
is obtained from specialized cells known as
specific use owing to their biological group of
compounds. Several species of the genus aloe pericyclictubules that occur just beneath the ep-
has been in use under the common name of aloe idermis or rind of the leaves.
viz. Aloe vera, Aloe barbadensis, Aloe ferox, Aloe vera plants products are biologically
Aloe chinensis, Aloe indica, Aloe peyrii, etc. active and hence their post harvest handling and
Amongst these Aloe vera Linn syn. Aloe processing needs great care. The time, tempera-
barbadensis Miller is accepted unanimously as ture and sanitation are the prime requirement for
the correct botanical source of aloe. Aloe vera a processing to put the Aloe vera plant products in
member of the lily (Liliaceae) family is a spiky, active form. The most important factor is the
succulent, perennial plant and a native to warm how to extract the gel from Aloe vera leaf and to
dry regions. It is popularly grown as indoors preserve it for long duration for its utilization in
plant and cultivated almost everywhere in the cosmetic and pharmaceutical products.
world, both as a houseplant and for its medicinal
qualities. There are about 300 identified species.
Aloe vera Gel is the colorless mucilaginous gel Handling of Aloe vera leaves
obtained from the parenchymatous cells in the Aloe vera barbadensis can grow up to 100
fresh leaves of Aloe vera (L) Burm. f. cm height, although most specimens are 30 to
(Liliaceae) (Gilman, 1999; Moore, 2001). 60 cm in height. It has thick leaves that grow in
a rosette shape. The parenchyma cells of the

*Corresponding author: (E-mail) vkchandegara <@> jau.in http://www.openaccessscience.com


2013 Copyright by the Authors, licensee Open Access Science Research Publisher. ijmap@openaccessscience.com
This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported (CC BY-NC-
ND 3.0) License (http://creativecommons.org/licenses/by-nc-nd/3.0)
493
Int. J. Med. Arom. Plants Aloe vera: a review
leaves contain large quantities of pulp. The added to Aloe solutions about 20-25 % of the
fleshy leaves with serrated edges that arise from total solids come out of solution or
a central base and grow to nearly 30 50 cm 'precipitate'. The chemical constituents of Aloe
long have 10 cm width at the base. vera barbadensis (Joshi, 1998) consists of main-
ly polysaccharides, glycoprotein and salts of
The plants can be harvested every 6 to 8
organic Acids. The polysaccharides represent
weeks by removing 3 to 4 leaves per plant. Aloe
about one-half to two-thirds of the MPS or
vera leaves are normally sensitive to subfreez-
about 10-15% of the total solids. (iii) Polysac-
ing temperatures The weather conditions are
charides: There are over 200 constituents in Al-
highly affect the Aloe vera processing schedule.
oe vera, the single most important constituent
Pulling back on the green leaf and cutting at the
being the polysaccharides.
white base carry out the harvesting of the Aloe
vera plant. To avoid bio-degradation the Aloe
vera leaf is harvested and pulled carefully from
Biologically active chemical constituents of Al-
the mother plant so as not to break the rind.
oe vera leaves
Biological activity loss is due to the micro- The gel contains 98.5 % water having pH of
bial decay of the gel. The first exposure of the 4.5 and also contains many polysaccharides
inner gel to microbes is when the leaves are
such as Glucomannan, Acemannan etc., in ac-
harvested from the plant. Leaves in which the
tive form in the leaves of Aloe vera.
base is not intact and sealed will greatly increase
Glucomannan is a good moisturizer and mainly
the microbial counts in the finished product.
used in many cosmetics products (Henry, 1979)
Higher level of microbial counts significantly
whereas Acemannan, the major carbohydrate
reduces the biological activity in the product.
fraction in the gel, is a water-soluble long chain
The other major source of microbial contamina-
mannose polymer which accelerates wound
tion comes from the rind of the leaf. The har-
healing, modulates immune function and antivi-
vested leaves were kept in the icebox at 4 -5 0C
ral effects.
and transported to the processing unit.

Processing parameters of Aloe vera


Aloe Vera leaf characteristics and composi-
tion Time, temperature and sanitation (TTS) are
necessary to preserve these biological activities.
Physical structure of Aloe vera leaf
The TTS Aloe Process not only preserves the
The Aloe Leaf consists of three layers: natural biological activities of Aloe vera but also
enhances the physical stability of the finished
A. The outer thick rind
products.
B. A viscous, jelly like mucilage layer into
which the vascular bundles, attached to the inner
surface of the rind, protrude. Timing of process
C. The fillet proper, which has structural integri- Leaves show losses of biological activity
ty consisting of hexagonal structures containing beginning at six hours following harvest when
the fillet fluid. This is the water storage area for the leaves are stored at ambient temperature.
the plant. Most biological activities are completely lost
after 24 hours at ambient temperatures. The
losses of activity appear to be the result of en-
Chemical composition of Aloe vera leaf zymatic activity after the leaf is removed from
The main constituents of the Aloe vera leaf the plant. In fact, it has been shown that the gel,
are: (i) Aloin: It is an irritant laxative contained once extracted from the leaf, has greater stabil-
in the yellow sap of Aloe, which is a constituent ity than gel, which is left in the leaf. This means
of the Anthraquinone complex, (ii) Methanol- that shipping of leaves, even at refrigerated
Precipitable Solids (MPS): When alcohols are temperatures, will result in loss of biological
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494
Int. J. Med. Arom. Plants Aloe vera: a review
activity. The overall timing of TTS production by spray drying or freeze drying (Waller et al.,
phases is extremely critical. The processing 2004). Freeze-drying involves placing frozen
must be completed within 36 hours of harvest- gel under a high vacuum. Water sublimes from
ing the leaves (http://www. aloecorp.com). the frozen gel as it gradually heats. Spray drying
is a two step process. The process begins with
matrix development. The matrix is pumped
Process Temperature through a spray dryer chamber. Fluid is sprayed
The Aloe gel processing temperature plays as a fine mist out a series of nozzles through this
very important role for gel quality for cosmetic chamber. The chamber is heated between 50 to
and medicinal use. 90 0C causing water to evaporate and the aloe
matrix to dry. With temperature playing a cru-
A. Flash Cooling cial role in maintaining natural plant products,
As a crucial step to preserve biological ac- freeze-drying is favoured. Heat is not added so
tivity, the gel is cooled to below 5 0C in ten to that chemical transformations are minimized
fifteen seconds following the gel extraction. and the biological activity of the gel is not alte-
Rapid cooling not only slows enzymatic and red as may be the case with spray drying.
microbial deterioration of the gel, but also aids Freeze drying of the Aloe vera fillets were at
in reducing the microbial counts in the product. low temperature under vacuum found the max-
B. Pasteurization imum value of rehydration ratio and water hold-
ing capacity (Andani, 2010).
Biological activity remains essentially intact
when the gel is heated at 65 0C for periods of Osmotic drying of Aloe vera (Aloe
less than fifteen minutes. Extended periods or barbadensis Miller) cubes were osmosed for 4
higher temperatures will result in greatly re- h in sugar syrup of different concentration and
duced activity levels. The best method of pas- temperatures at constant syrup to fruit ratio of
teurization is HTST (high temperature short 5:1. Drying of Osmosed and unosmosed Aloe
time), which exposes the gel to elevated temper- vera samples at different temperature with con-
atures for periods of one to three minutes. Once stant air velocity, observed water loss and solid
heated, the gel is flashing cooled to 5 0C or be- gain during osmo-drying. (Simal et al. 2000,
low. Chang et al. 2006, Vega et al.2007, Segovia et
al. 2009 and Pisalkar et.al. 2011).
C. Concentration
The gels obtained using the pasteurization
and flash-cooling methods can be concentrated Processing of Aloe vera
under vacuum without the loss of biological ac- The potential use of Aloe vera products of-
tivity. The concentration operation must be con- ten involves some type of processing, like heat-
ducted under 125 mm mercury vacuum at tem- ing, dehydration and grinding (Chang et al.,
peratures below 50 0C and must not exceed two 2006). Unfortunately, because of improper pro-
minutes. Higher vacuums and temperatures will cessing procedure aloe products contain very
cause activity loss as will extend concentration little or virtually no active ingredients
times. (Ramachandra and Rao, 2010), so it has become
D. Drying very important to evolve a better method of
preservation for increasing the shelf life and
The concentrated product can then be freeze maintaining the quality of Aloe vera gel.
dried at temperatures between -45 0C and 30 0C
or can be spray dried with product temperatures
below 60 0C without losses in biological activi- Washing of Aloe vera leaf
ty. For export purposes (especially for cosmetic
industry), dried Aloe gel is favoured. Gel fillets When Aloe vera leaves are harvested, it con-
can be directly dried by dehydration under a low tains dirt and other impurities. The yellow fluid
heat. However, gel liquid is mostly dried either secretion from the harvested leaves should be
completely removed from the leaf for its pro-
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495
Int. J. Med. Arom. Plants Aloe vera: a review
cessing and purity of products. The leaves were lage layer below the green rind avoiding the
thoroughly washed with fresh water with me- vascular bundles and the top rind is also re-
chanical washer. In the Aloe vera processing moved with the help of knife. The bottom rind
industry, leaves are initially washed in a steriliz- is similarly removed.
ing solution, a 200 ppm solution of sodium hy-
The hand - filleting method of processing
pochlorite (Waller et al., 2004). If leaves are
Aloe leaves was developed to avoid contaminat-
extremely muddy when delivered to the gel fac-
ing the internal fillet with the yellow sap. In this
tory they are pre-washed in a basin of deionised
method the rind is removed by using sharp
water. In some cases, the pre-wash step involves
knife, keeping anthraquinone level low, but in
scouring the leaf rind with soft brushes
this process the most of the mucilage is left on
(McAnalley, 1990).
the working table. During processing operation,
the lower 25 mm of the leaf base (the white part
attached to the large rosette stem of the plant),
Pre-treatment for Aloe vera processing
the tapering point (50 100 mm) of the leaf top,
The Aloe vera leaves are preconditioned by and the short, sharp spines located along the leaf
sun drying, shade drying and by steaming. The margins are removed with the help of sharp
study revealed that, two days sun or shade dry- knife. The knife is then introduced into the mu-
ing, yielded highest crude gel recovery and less- cilage layer below the green rind to remove top
er residual time without aloin contain as com- rind and similarly the bottom rind is removed
pared to the fresh leaves el. They have also re- (www.bonasana.com).
vealed that the matured leaves lead more crude
gel recovery as compared to immature leaves.
The immature leaves take more time in pro- Mechanical filleting method
cessing by manually as well as mechanically for
Mechanical filleting is the most commonly
gel extraction (Anonymous, 2008a).
used method in the industry for gel extraction
Study on gel extraction efficiency by taking from the Aloe vera leaves (Obrien, 2005). This
different pretreatments such as brine, lye, water process takes place on a conveyer belt, equipped
and without treatment i.e., control found that with rollers and blades. Initially, the leaf (upper
scrapper method with brine treatment is most surface facing downwards) is passed over a
suitable for extraction of gel that gives 93.42 % blade mounted on a table. The upper rind is cut
gel extraction efficiency (Anonymous, 2008c). away in one swift movement. The exposed gel
surface is then longitudinally sliced from the
upper to lower surface but not completely
Peeling of Aloe vera leaf through the lower rind surface so that the curved
The removal of outer skin and rind is the lower rind becomes flat. The lower rind can
most tedious operation for mechanical machine now be easily removed by passing it over the
due the shape of Aloe vera leaf. Precautions blade as before. The gel slices are then collect-
should be taken to avoid contamination of inner ed. The next step in gel processing is the remov-
part with exudates secretion to maintain purity al of cellular material from the gel. The gel fil-
of products. lets are chopped into small chips and de-pulped
using sieves3. It can also be liquidized as in the
fruit juice industry and filtered to remove cellu-
Hand filleting lar material. The liquid gel is obtained, only af-
ter the removal of fiber. The gel in the crude
In order to avoid contaminating the internal form is sold as a commercial product. For the
fillet with the yellow sap, the lower portion i.e. long term storage the gel is mixed with activated
25 mm of the leaf base (the white part attached charcoal for purification and then filtered. It can
to the large rosette stem of the plant), the taper- also be preserved, by putting some stabilizing
ing point (50 100 mm) of the leaf top, and the agent. The treatment with activated charcoal
short, sharp spines located along the leaf mar- ensures that any anthraquinone compounds in
gins are removed by a sharp knife. The muci-
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496
Int. J. Med. Arom. Plants Aloe vera: a review
the gel are removed. In the A. vera industry, pair of rollers with variable apertures are ar-
0.05 % w/v charcoal is added to 2000 L gel, ap- ranged to accommodate the varying width and
proximately gel takes one hour to pass through thickness of the Aloe vera leaf. The purity is not
Celite Filteraide for filteration. maintained in this method of peeling as there is
mixed of outer exudates with inner pulp.

Whole leaf processing In the roller method of gel expulsion, the


leaves are passed through rollers and the fillet
In this process, the base and tip are removed pops out, same time more pressure is applied
and then the leaf is cut into sections and ground to the pericyclic tubules for gel expulsion. A
into particulate slurry. The material is then low cost gel extractor had developed comprising
treated with chemicals, which breaks down the of two roller having diameter 118 mm and
hexagonal structure of the fillet releasing the length of 245 mm with one roller has continuous
constituents. Then by expression and extraction, slope (Anonymous, 2008a). Similarly, low cost
the undesirable elements can be selectively re- Aloe juice extractor has also developed (Anon-
moved, while maximizing the desired constitu- ymous, 2008b). Similar machine developed hav-
ents. This process, performed properly, can pro- ing two stainless steel roller rotated with chain
duce a constituent-rich juice (generally contain- and sprocket (Anonymous, 2008c).
ing 3 times or more constituents than hand fil-
A 60 80 kg leaves/h capacity, Aloe vera
leted juice), which should be virtually free of
gel (fillet) extractor was designed and developed
the laxative anthraquinones; this process was
by providing adjustable gap in between the
developed in the 1980s
crushing rollers, so that only the gel is just ex-
(http://www.wholeleaf.com). The data of hand
tracted and over crushing of the leaves can be
and whole leaf filleting which reveals that the
avoided(Anonymous, 2008d) .
quantity of desirable polysaccharides is 2.5 to 3
times higher as compare to hand filleting meth- An apparatus for extraction of uncontami-
ods (Table 1). nated Aloe vera gel from the leaves of Aloe vera
plants had developed in which the harvested
In the method of whole leaf processing, the
leaves of the Aloe vera plants are placed be-
whole leaf is coarsely chopped and the rind par-
tween a pair of endless moving belts. The leaves
ticles are removed by passing through filters of
are passing through a number of crushing rollers
various porosities. The anthraquinone are re-
arranged in a desired pattern. The rollers first
moved by using charcoal. This method produces
crush the core of the leaf to enable the gel to
a product rich in carbohydrates but also much
flow internally while a second set of rollers ex-
higher in mineral salts than the other methods
trudes the gel from the leaf. The crushed leaf
(Danhof, 2000).
and extruded gel is then fall on a drain grate to
enable gravity flow for the separation of gel
Table 1: Effect of leaf processing method on from the crushed leaves. The proper slope is
yields and constituents. provided to the drainage grate, so that the leaves
will slowly move across the drain grate to ena-
Process Fraction Hand Filleting Whole Leaf ble separation of the gel. The leaves are re-
(%) (%)
Total solids (Without pre- 0.45 0.65 1.30 3.50 moved from the gel collection area before it
servatives or additives) mixes with the flowing aloin to avoid contami-
Polysaccharides 0.12 0.16 nation (Tumlinson, 1985).
Source: http://www.wholeleaf.com

Aloe vera leaf splitter


Roller squeezing method Aloe vera leaf splitter is very advance meth-
In this method of peeling the Aloe vera leaf od of peeling in which, leafs are spitted by me-
is passed between two parallel rollers rotating in chanical machines that simulates hand filleting
opposite direction and at different speed. The operation.

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497
Int. J. Med. Arom. Plants Aloe vera: a review
A thin wire is used to split the Aloe vera structure for peeling the lower rind panel from
leaf, which can be placed at varying distances an Aloe vera leaf whose ends and side marginal
from the vascular bundles. The wire is allowed portions have been removed while the fourth
to go too close to the rind, the extracted gel will station includes structure for removing the gel
contain more anthraquinone as well as more of layer of the leaf disposed on the upper rind pan-
the mucilage, if it is too close to gel fillet, and el thereof and exposed by the removal of the
then less anthraquinone as well as less mucilage lower rind panel of the leaf (De Gray, 1986).
will be obtained.
Aloe vera gel extracting apparatus, which
Aloe vera plant leaf to a cutting knife of de- consists of a body, transmission system, peeling
veloped apparatus. The apparatus is designed to device and a driving mechanism. The transmis-
transport the leaf on an endless belt conveyor on sion system comprises an upper and a lower
which the leaf is laid down flat and lengthwise part. The upper part of the system connected to
on the conveyor belt. A second endless belt the body through the belt sheave axle at the
conveyor travels in the same direction and at the right end and the belt sheave axle at the left end
same speed as the first endless belt conveyor but connected to the hanger trestle in synchronous
is disposed at a right angle to the first endless vertical movement with it. The lower part of the
belt conveyor at the feed end of the apparatus. system connected to the body at both ends
The first endless belt conveyor in its travel is through the sheave axles. The peeling device
slowly twisted towards the second endless belt consists of an edge cutting blade and a peeling
conveyor and by the time the first endless belt blade. The edge of cutting blade is set in the slot
conveyor has reached the end of its travel, the between the two groups of belt. The upper peel-
leaf has been turned from a flat condition to a ing blade is connected to the hanger trestle and
vertical position and is sandwiched between the the lower peeling blade is connected directly to
two sets of endless conveyor belts. The leaf now the body (Xiaozhou, 2000).
standing on its edge between the aforesaid sets
of endless belt conveyors, the same is fed into
the apparatus where the leaf are cut into two Data comparison of various processing methods
half and thereafter the gel within the leaf will be The data comparison of various processing
squeezed and recovered (Thompson, 1983). methods and the effect on yield (total solids),
In developed a method and apparatus for ex- aloin concentration, and the distribution of sizes
tracting gel from Aloe vera leaves without con- of constituents (Table 3). The whole leaf meth-
taminating the gel with toxic juices, the Aloe od can produce an Aloe juice, which is rich in
vera leaves are washed, trimmed, and fed to the total solids however; the aloin concentration is
hopper. The leaves will undergo to and through at a very low acceptable level.
motion of a blade, which longitudinally bisects
the leaves. The split leaves are then passed
through pressing rollers, which advance the rind Table 2: Comparison of various processing
but retain the gel that falls from the pressing methods and constituents.
rollers into a collection pan (Cottrell, 1984). Method of pH Aloin, Per cent, Per cent,
Preparation (ppm) H20 Total Solids
An elongated conveyor assembly on which Hand- filleting 4.27 6 99.25 0.48
an Aloe vera leaf is lengthwise disposed and ad- Roller 4.30 32 99.61 0.39
vanced from one end of the conveyor to the oth- Leaf Splitter 4.24 18 99.61 0.42
er end. The first and second cutting stations are Whole Leaf 4.09 1 98.62 1.38
spaced along the conveyor assembly. They re- Source : http://wholeleaf.com
move the opposite ends of an Aloe vera leaf and
also trim the serrated edges of the leaf. In addi-
tion to this, the third and fourth stations are dis- Commercial production
posed along the conveyor assembly between the Total process of Aloe vera
second station and the discharge end of the con-
veyor assembly and the third station includes
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498
Int. J. Med. Arom. Plants Aloe vera: a review
In this process, aloe leaves are hand filleted calcium, magnesium, and malic acid, which are
by the traditional method. Then the green rinds virtually free from undesirable laxative
and the mucilage pulp are processed separately. anthraquinones. The International Aloe Science
A combination of the products obtained by these Council for certification recommends using the
two procedures, produces a product called Total total process Aloe, which retains major portion
Process Aloe. Total Process Aloe contains con- of desirable constituents.
siderably higher concentrations of total solids,

Figure 1: Commercial Aloe vera processing flow chart.

ALOECORP Process boxes, which are transported immediately to the


production facility. The incoming harvested
The outermost matured three leaves are cut
leaves are fed into the primary washer located
from every plant. The leaves are gathered in
just outside the production room. The produc-
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499
Int. J. Med. Arom. Plants Aloe vera: a review
tion room is having stainless steel conveyor sys- Gel extraction by Centrifugation
tem that quickly moves harvested leaves from
In this method the whole leaf after removal
the primary wash tank to processing room. The
of the peel the colourless hydroparenchyma
conveyors propel leaves to the mechanical leaf
was ground in a blender and centrifuged at
washer, then to the cutting area, and finally
10,000 x g for 30 min at 4 0C to remove the fi-
through the gel expulsion machines
bers. Two other patented processes to obtain
(http://www. aloecorp.com).
gel are commonly used in the aloe industry. The
The other processes which are commonly first is a method to extract gel polysaccharides
used to obtain gel in the Aloe industry is by al- by alcohol precipitation (www.bonasana.com).
cohol precipitation. In this process, 20 gallons As described in the (McAnalley, 1990) patent,
of Aloe gel are pumped into 100 gallon tanks, 20 gallons of aloe gel are pumped into 100 gal-
and then ethanol (80 gallons) is added to the Al- lon tanks. Ethanol (80 gallons) is added to the
oe gel and stirred for 20-30 minutes. The alco- aloe gel and stirred for 20-30 minutes. The al-
hol-Aloe gel mixture is then left for condition- cohol-aloe gel mixture is then left to stand for
ing for four hours. The clear supernatant that four hours. The clear supernatant that forms is
forms is decanted or siphoned off without dis- decanted or siphoned off, without disturbing the
turbing the precipitate on the bottom of the tank. precipitate on the bottom of the tank. The solu-
The solution is then placed into centrifuging tion is then placed into centrifuging buckets and
buckets and centrifuged. The precipitate formed centrifuged. The precipitate formed is collected
is collected and washed with fresh ethanol. This and washed with fresh ethanol. This fraction is
fraction is then freeze-dried. then freeze-dried. The second process is used in
the Aloe ferox industry in combination with al-
cohol precipitation developed (Botha, 1994).
Gel extraction process from Aloe vera pulp The pulp remaining after liquidised aloe gel is
The gel extraction from Aloe vera leaves, filtered is used for this process. This pulp is
had been carried out by removing of its exudates treated with sodium citrate that results in the
and its mucilage was scraped out with blunt freeing of polysaccharides from calcium. Water
edged knife. This mucilage was stirred vigor- is added and the mixture is heated. This mixture
ously in a blender to make it uniform. This solu- is then filtered, and the liquid fraction, which
tion was strained through a muslin cloth and fil- contains the calcium free polysaccharides, is
tered. This uniform solution was extracted for known as aloe jelly. Careful storage of gel
cold- extracted gel (CEG) and hot extracted gel (liquid or powder) is important to prevent loss
(HEG). of quality. Relative humidity and temperature
affect product quality and shelf life (He et al.,
2004). Freeze dried gel has to be packaged in
Cold extracted gel (CEG) airtight containers or kept under dry conditions
as it rehydrates rapidly (Femenia et al., 2003).
This solution was acidified with Hydro chlo-
ric acid (HCL) having pH 3.50 and the crude gel A developed process for extraction of gel
were precipitated out from the extract by adding by manual peeling of leaf and principle of cen-
slowly 95 % alcohol while stirring. The gel was trifugation applied is shown in Figure 2.
obtained by centrifugation.
Purification of Aloe vera gel
Hot extracted gel (HEG) The next step in gel processing is the re-
Material left after passing the blended solu- moval of cellular material from the gel. Gel fil-
tion through muslin cloth, was repeatedly treat- lets are chopped into small chips and de-pulped
ed with hot water until the complete extractions using sieves. Gel fillets can also be liquidised as
of gel was affected. The crude gel (HEG) was in the fruit juice industry and filtered to remove
prepared as described as above. cellular material. After removal of the fibre, on-
ly the liquid gel remains. The gel in this crude
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Int. J. Med. Arom. Plants Aloe vera: a review
form is sold as a commercial product, but may any anthraquinone compounds in the gel are
also be mixed with activated charcoal, filter removed. In the A. vera industry, 0.05 % w/v
pressed, stabilized (preserved) and dried. charcoal is added to 2000 L gel.
Treatment with activated charcoal ensures that

Figure 2: Aloe vera Gel Extraction by Centrifugation Process Flow chart (Chandegara, 2005).

Aloe vera gel characteristics and composition and shown in Table 4. This meets or exceeds the
standards established by the International Aloe
Physico-chemical properties of Aloe vera gel
Science Council's (IASC) certification program
Following companies had reported the for the determination of purity.
physico-chemical properties of Aloe vera gel

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Int. J. Med. Arom. Plants Aloe vera: a review
Table 3: Fractionation of Aloe vera Gel Extrac- Aloe vera gel has a biologically active poly-
tion Process (Chandegara, 2005). saccharide known as acetylated mannose, or
Aloe leaf weight 1.000 kg acemannan. Acemannan is one of many saccha-
Aloe pulp weight 0.501 kg (50.04 % of Aloe vera leaf) rides contained in Aloe vera. Some of the others
Crude gel recovery 0.211 kg (42.17 % of pulp) are arabinose, cellulose, galactose, mannose,
Pure gel recovery 0.106 kg (50.17 % of crude gel re- and xylose. Prostaglandins are a third important
covery) set of compounds, and are thought to play a ma-
jor role in wound healing. Aloe vera also con-
Chemical composition of Aloe vera gel tains fatty acids, enzymes, amino acids, vita-
mins, minerals, and other substances.

Table 4: Physico-chemical properties of Aloe vera gel.


Test AloeCORP M/s Delta International
http://www. aloecorp.com http://www.garudaint.com
Appearance Clear Yellow / Green Liquid
*Absorbance @ 400nm NMT 0.500
Refractive Index 1.3340-1.3355 1.33789 - 1.34390
Specific Gravity 1.0030-1.0070 1.0221 - 1.0339
pH Value 3.5-4.7 3.5 - 4.7
Total Solids NLT 0.46% by weight

Table 5: Aloe gel composition.


Mono and polysaccharides (50-60% of solids)
(Specific concentrations have not yet been determined)
Ployhexanoses Hexans Xylose Arabinose Galactose Glucose
Amino acids (ppm)
Lysine 5-6 Histadine 2.8-3.3 Arginine 4.5-5.5
Threonine 5-6 Aspartic Acid 13-15 Serine 6-7
Glutamic Acid 13.5-15.5 Proline 8-9 Analine 1.0-1.3
Glycine 7-8 Valine 6.5-7.0 Methionine 1.5-2.0
Isoleucine 3.5-4.0 Leucine 8.5-9.0 Tyrosine 2.8-3.3
Pheylalanine 4.3-4.7
Vitamins (mg per 100ml)
B-1 6-7 B-2 6-7 C 47-61
Niacinamide 30-37 B-6 3.0-3.7 Choline 9.5-11.2
Enzymes (per 100 ml)
Amylase 1100-1600 units Lipase 600-800 units
Protein 0.11g / 100 gr Fat 0.09g / 100 gr
Ash 0.25% Crude fiber 0.10%
Calories 3.3/100 gr
Source: http://www.garudaint.com

Quality parameters of Aloe vera gel A. Fiber content


The quality parameters such as fiber content, The fiber content is directly related to the
viscosity, refractive index, optical density and purity of gel and become the criteria of efficien-
total soluble solid plays an important role in cy of gel filtration unit. More fiber content, sug-
judging the quality and purity of extracted gel gests poor filtration operation. The difference
from Aloe vera leaf. between crude gel recovery and pure gel recov-
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502
Int. J. Med. Arom. Plants Aloe vera: a review
ery gives the amount of fiber in crude gel. It had ried out. The solution was then stored at room
been found that the fibre content 0.074 to 0.088 temperature for 6 months for observations of the
% of fresh weight of pulp (Wang and Strong, structure and homogeneity of the polysaccha-
1993). rides. Addition of the algal sulphated polysac-
charide resulted in a homogeneous stable prod-
uct: the algal polysaccharide may inhibit degra-
B. Viscosity dation and also browning of the aloe polysac-
Viscosity of gel is very important factor for charide (Yaron, 1992).
deciding quality in terms of activities of biolog-
ical compounds. The viscosity decreases as the
time passes. After harvest of Aloe vera leaf, the Product preparations from Aloe vera
viscous pseudoplastic nature of Aloe vera gel, Aloe vera is an industrial crop and in the
mainly due to the presence of polysaccharides food industry it has been utilized for the prepa-
composed of a mixture of acetylated ration of health food drinks, beverages like tea,
glucomannans is lost shortly after extraction, milk, ice-cream and confectionary (Seoshin et
apparently due to enzymatic degradation al., 1995). Aloe vera gel also finds application in
(Gowda et al., 1979). These shows there are cosmetic and toiletry industry for the prepara-
some biological activities, which related to the tion of creams, lotions, soaps, shampoos and
viscoelastic behavior of gel. facial cleaners (Grindlay and Reynolds, 1986).
Choosing effective Aloe vera products can be
challenging. Once a leaf is cut, enzymes start to
C. Refractive index break down some of the long chain sugars
Refractive index is the physical property of which make Aloe vera gel an effective healing
gel determines the purity of gel as compared to product, so it is important for the plant to have
double distilled water. Gel with lowest refrac- been properly handled and stabilized. Commer-
tive index, is the best treatment for extraction cial, stabilized gel products may not work as
process. well as the fresh gel, but cold processing is
thought to best retain the beneficial properties.
Aloe vera juice is most often the form of the gel
D. Optical density that is used internally.
Optical density is the physical property of
gel determines the purity of gel as compared to Aloe vera dessert
double distilled water. Gel with lowest optical
density, is the best treatment for extraction pro- Basically, the aloe desserts processing pro-
cess. More optical density indicates the impuri- cess is simple which involved sorting, grading,
ties in the extracted gel. The optical density of washing, peeling, cutting, cooking in syrup,
1.020 to 1.437 (abs) for Aloe vera leaves were adding flavor, packing, and pasteurizing. The
reported (Wang and Strong, 1993). most difficult part of processing is the removal
of aloe and retains its original taste and its mar-
ketability. The flow chart of commercialized
Stabilization of Aloe vera gel processing of Aloe vera is shown in Figure 3
(Herlina, 2001).
Many of the greatest benefits of Aloe vera
can be lost in the processing unless great care is
taken to stabilize the gel. Aloe vera gel, like Salve: Remove the thin outer skin and process
most natural juices, both fruit and vegetable, is the leaves in a blender, add 500 units of vitamin
an unstable product when extracted and is sub- C powder to each cup and store in refrigerator
ject to discoloration and spoilage from contami- (Herlina, 2001).
nation by microorganisms. Stabilization of Aloe
vera gel with Sulphated polysaccharides of the
red microalga Porphyridium aerugineum is car-
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Int. J. Med. Arom. Plants Aloe vera: a review
Dried Juice: Aloe vera juice containing the The processing of Aloe vera requires critical
equivalent of 360 - 900 mg of dried sap is rec- attention in time, temperature and sanitation.
ommended by most herbalists per day (Herlina, The processing and handling should be carried
2001). out at low temperature to preserve its active in-
gredients. The quality of Aloe vera gel should
be evaluated in terms of quality parameters like
Aloe tea and fibre tablets: Dry aloe leaves are viscosity of gel, optical density, and refractive
harvested and crushed to form tea leaves. A de- index. Aloe vera gel expulsion by splitting of
licious herbal tea can be brewed. Tea leaves are leaf, roller squeezing method, crushing of whole
pressed to form fibre tablets (Herlina, 2001). leaf, hand filleting methods and mechanical fil-
leting methods. Aloe vera gel should be freeze
dried to maintain biological properties as it con-
tains active compounds. After extracting the gel,
the stabilization of gel is inevitable for its long
duration storage and product formulations. Pre-
sent processing techniques aims at producing
best quality aloe products but end aloe products
contain very little or virtually no active ingredi-
ents. Hence, appropriate processing techniques
should be employed during processing in order
to extend the use of Aloe vera gel.

Figure 3: Processing process of Aloe vera


Dessert.

Conclusions
A review from different cited reference on
processing of Aloe vera leaf gel has revealed
some useful information. Aloe vera plant has
potential in pharmaceutical, nutritional and
cosmetic industries. The leaf of Aloe vera plant Figure 4: Flow chart with mass balance for
contains biological active compounds, which preparation of jelly from Aloe vera gel (Anon-
needs careful harvesting and handling. Tem- ymous, 2008a).
perature is the main factor for processing of Al-
oe vera and particularly gel extraction process.

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504
Int. J. Med. Arom. Plants Aloe vera: a review

Figure 5: Flow chart with mass balance for preparation of Aloe vera gel blended RTS Beverage
(Annonymous, 2008a).

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