Enriched aqueous components of emblica officinalis

Abstract

In an extraction process comprising extracting a raw extract from Emblica officinalis the improvement comprising conducting the extraction under conditions of time, temperature and atmosphere, to inhibit the formation of black specks and/or oligomeric and/or polymeric tannins and/or oxidation products thereof.

Description

SPECIFICATION

[0002] This invention relates to methods of eliminating undesired substances, including but not limited to oligomeric/polymeric components from compositions obtained from the fruit of Emblica officinalis plant also known as Phyllanthus Emblica and the resulting enriched compositions. This plant is generally found in India, China, Pakistan, Nepal and other countries. Accordingly, this invention is directed to extracts of Emblica officinalis from any geographical location.

[0003] Compositions obtained from an extract of the fruit of the Emblica officinalis plant have been described in the prior art, for example, in the above cross-referenced allowed application Ser. No. 10/120,156, the references referred to therein, as well as in U.S. Pat. No. 6,235,721 issued May 22, 2001 and U.S. Pat. No. 6,636,162 issued Mar. 26, 2002.

[0004] In U.S. Pat. No. 6,235,721, an anti-oxidant product referred to as “CAPROS” is isolated from the fruit of Emblica officinalis plant using a very dilute aqueous or alcoholic water salt solution, e.g. a 0.1 to 5% (w/w), preferably 1 to 2%, of a sodium chloride, potassium chloride, calcium chloride or magnesium chloride solution, which prevents degradation of the anti-oxidant compounds therein by enzymes present in the fruits of the Emblica officinalis plant. Alternatively, the anti-oxidant product is isolated using a buffer solution, e.g. 0.1 to 5% (w/w), preferably 1 to 2%, of sodium citrate/citric acid, sodium acetate/acetic acid, sodium phosphate/phosphoric acid, instead of aqueous or alcoholic water salt solution. It is further stated in this patent that the composition contains, by weight, Embilcanin-A and B (gallic/ellagic acid derivatives of 2-keto-glucono-δ-lactone) (35-55%), Punigluconin (2,3-di-O-galloyl-0,6-(S)-hexahydroxy-diphenoylgluconic acid) 4-15%), Pedunculagin (2,3,4,6-bis-(S)-hexahydroxydiphenoyl-D-glucose) (10-20%); Rutin (flavanol-3-)glycoside (5-15%); low to medium molecular weight gallo-ellagi tannoids (10-30%); gallic acid (0-5%) and ellagic acid (0-5%).

[0005] In the cross referenced allowed application Ser. No. 10/120,156, a standardized composition is described which is useful, for example, in skin lightening or skin whitening. This composition, hereinafter, termed “EMBLICA” is distinguished from “CAPROS”, by, for example, having less than 1% by weight of total flavonoids and even lower contents of RUTIN. Whereas, light colored EMBLICA consists essentially of the desired components for the purposes of skin lightening or skin whitening, it has been observed that black specks in the commercial product diminish the esthetic appearance of the final formulations. Other commercially available products based on extracts of Emblica officinalis are even darker in color due, on information and belief, to the presence of a larger number of black specks and water-insoluble oligomeric/polymeric materials.

[0006] Accordingly, one aspect of this invention is to provide at least one process for the removal of black specks in all types of extracts of Emblica officinalis so that the resulting composition is macroscopically (visually) devoid of such specks.

[0007] Another aspect of this invention is to provide a material substantially devoid of water-insoluble oligomeric/polymeric components.

[0008] We have discovered that the black specks are substantially, if not completely water-insoluble as measured at room temperature, (20-25° C.). A chemical analysis of these specks reveals that they comprise oligomeric/polymeric tannoids having no aromatic hydrogen.

[0009] We have also determined that the black specks have a particle size of on the order of about 20 μ down to 1 micron. Thus, it has been observed that some black specks pass through a 5 micron filter but hardly any pass through a one micron filter.

[0010] Without being bound by an explanation of the cause of the black specks, it is believed that the black specks are oxidation products, likely of phenolic hydroxy groups and/or oligomeric or polymeric tannins especially those having a molecular weight of above on the order of 3000.

[0011] We have discovered that such black specks and also oligomeric and polymeric tannins are substantially, if not completely water-insoluble, and that they are biologically inactive materials.

[0012] Thus, another aspect of this invention is to provide at least two processes which will remove the water-insoluble oligomeric and polymeric tannins, especially such tannins having a molecular weight of over 1000 and particularly over 3000 (hereinafter referred to as polymeric tannins). By water-insoluble it meant that a 1% by weight concentration of polymeric tannin in water does not exhibit a solubility of more that 10% by weight of the total tannin at 22° C.

[0013] Still another aspect is to provide substantially water-soluble (over 95% by weight) extracts of Phyllanthus Emblica comprising, for example, less than 5% by weight of polymeric tannins, with substantially no black specks and at high levels, e.g. over 75% by weight of bio-active, low molecular-weight hydrolysable tannins having molecular weights below 1,000. The resultant extracts can be used for all applications previously described in the prior art: e.g. in cosmetic formulations, for example, skin lightening or even-toning, anti-aging and sunscreens, as well as in nutritional supplements and any new applications developed in the future.

[0014] Upon further study of the specification and dependent claims, further aspects and advantages of the inventions will become apparent.

[0015] To attain the objectives of the invention, there is provided at least one process which comprises preventing the formation of black specks and/or precursors thereof and/or polymeric tannins. Also provided is at least one process for separating the black specks and/or precursors thereof and/or the polymeric tannins from the remainder of the components of extracts of Emblica officinalis.

[0016] In general, the invention process comprises the following steps:

[0017] 1) Providing an extract of Emblica officinalis either resulting from the original extract from the plant, or from a suspension of a powdered composition obtained after the extract is processed, e.g. after a drying step.

[0018] 2) If necessary, physically separating the black specks and/or precursors thereof and/or polymeric tannins from the water-soluble components, for example by filtration with the use of a filter aid.

[0019] 3) If desired, concentrating the resultant aqueous solution of the enriched composition of Emblica officinalis, for example to a dry powder.

[0020] With respect to step (1), if it is to be subjected to step (2), it is preferred to mix the raw extract or powdered extract with an aqueous solution preferably water. (By aqueous solution is meant water or mixture of water and a miscible solvent.) It is further preferred that the suspension contain about 5-30% more preferably about 18-22% by weight of total solids (including both dissolved and non-dissolved solids), and more preferably about 18-22%. When the extract is obtained from the fruit, the extraction is preferably conducted, under conditions so as to substantially prevent formation of polymeric tannins, e.g. low temperature (about 20° C. to 60° C.) and/or preferably under a substantially non-oxidizing atmosphere, e.g., the pressing apparatus is continuously flushed with nitrogen, and/or the addition of an autooxidation inhibitor, e.g. a saline solution. Likewise, the drying step is preferably conducted under conditions of temperature, time and atmosphere so as to mitigate the formation of black specks and/or polymeric tannins, examples of such conditions including but limited to drying at low temperature (freeze drying), short residence times in the spray drier, for example up to about 1 minute) and drying under vacuum at temperatures below 50° C.

[0021] If step (1) is nevertheless conducted under such conditions as to form black specks and/or precursors thereof, and/or polymeric tannins, it is necessary to conduct step (2).

[0022] As for step (2), the preferred separation method will take into account the physical and/or chemical properties of the black specks and/or precursors thereof. For example, as indicated above, in “EMBLICA”, the black specks have a particle size of approximately, of about 20 μ or less.

[0023] Ideally, it would be preferred to provide a method of separation which retains the bio-active components of EMBLICA by removing only the undesired components. Whereas there are a variety of separation procedures that can be employed, e.g. any one of a number of well-known filtration or centrifugation processes or combinations thereof, it is also contemplated that still other separation processes can be employed such as, for example, sedimentation, flotation and elutriation. A filter aid, e.g. diatomite filter aids, cross-linked polyvinyl pyrrolidone as well as silica and silicate sorbents can also be used to remove the oligomeric/polymeric materials. Some of the suppliers of these filter aids are Advanced Minerals (Celpure 25, 65 & 100, AW Cellite NF, MP Harborlite), International Specialty Products (Plasdone XL), United Perlite Corporation (Ultralite Perlite 505, 606C, 606F, 808, 909C, 909F). Likewise, extraction of the black specks or precursors thereof with a substantially water-miscible solvent, e.g. (ethanol, methanol, isopropanol or mixture of solvents) is also contemplated. For further details of separation systems, reference is made to descriptions in the patent and chemical engineering literature, for example, section 19 (liquid-solid systems) in Perry's Chemical Engineer's Handbook, 6th edition, editors Perry, Green and Maloney, 1984, McGraw-Hill Book Company.

[0024] With respect to step (3), a concentrated composition of water-soluble EMBLICA components can be produced by any number of conventional chemical engineering drying techniques. e.g. those described in Section 20 of Perry's Chemical Engineer's Handbook, 6th edition, and including but not limited to tray dryers, rotary dryers, agitated dryers, gravity dryers, vibrating-conveyor dryers, pneumatic conveyor dryers, Glatt dryers, freeze dryers and spray dryers. It is contemplated that prior to the drying step that the aqueous solution of the desired Emblica offinalis components can optionally be subjected to evaporation under sufficiently low temperatures so as to not to deleteriously affect the components. In view of the nature of the components, it is contemplated in order to forestall decomposition during drying that drying under vacuum, e.g.—freeze drying, will be preferred over a high temperature spray drying technique.

[0025] Without intending to be bound by the chemical structure, the water-insoluble oligomeric/polymeric components of Phyllanthus emblica extract appear to be based on the following general structure of monomeric units: 1

[0026] wherein R represents OH or ═O; and C-2/C-3 can have an unsaturation.

[0027] The arrow heads indicate the points of substitution meaning a fully aromatic-substituted product. The substituted moieties comprise other monomeric units which can be attached via a C—C bond and/or a C—O bond.

[0028] As for the evidence of the above depicted structure, the 300 MHz 1H-NMR spectrum of the acetylated product, in CDCl3 showed complete absence of Aromatic H signals. It is important to note that these oligomeric/polymeric tannins may create adverse health problems as they can combine irreversibly with some proteins. Hence, their presence is to be avoided.

[0029] One process to avoid the formation of oligomeric/polymeric tannins comprises the introduction of a small amount of salt solution, preferably sodium or potassium chloride, during the processing of the fruit juice. This salt solution inhibits the facile autooxidation of the small gallo-ellagi tannins into oligomeric/polymeric tannins. In addition to sodium or potassium chloride, it is contemplated that the addition of any non-reactive, soluble, ionizable compounds will increase the ionic strength of the reaction solution and will therefore inhibit oligomerization/polymerization.

[0030] By substituting the enriched compositions of Emblica officinalis produced by the present invention for the non-enriched Emblica extracts, substantial advantages are obtained. Examples of such compositions include but are not limited to skin and personal care compositions, e.g. sunscreens, as well as pharmaceutical and nutritional compositions.

[0031] Without further elaboration, it is believed that one skilled in the art, can, using the preceding description, utilize the present invention to its fullest extent. The following embodiments are, therefore, to be construed as merely illustrative and not limitative of the remainder of the disclosure in any way whatsoever. (These embodiments have not been necessarily actually conducted or prepared.)

EXAMPLE 1

[0032] A 20% by weight of an aqueous dispersion of EMBLICA powder was prepared by mixing the EMBLICA in water in a stainless-steel container with a hand-held agitator for about 15 minutes in order to obtain an uniform dispersion.

[0033] The properties of the EMBLICA powder, were as follows:

[0034] Low molecular weigh tannins—77.8% by HPLC

[0035] Water insoluble material—12.2%

[0036] Pale yellow powder

[0037] The resultant dispersion was then subjected to centrifugal filtration using a centrifuge (Heinkel HF 300, bowl diameter 300 mm, filter area 0.1 m2). 3L of a 10% solution of EMBLICA were filtered at a centrifuge speed of 1500 rpm. The filtration was complete within 10 min and yielded the following curve of weight filtration. The filter cloth porosity was 5 μm.

[0038] Filtered material was dried to a powder using a spray drier.

EXAMPLE 2

[0039] Using the same centrifuge employed in Example 1, two tests were performed at a 33% by weight concentration of EMBLICA in purified water but with different centrifugation speeds, i.e. different g forces applied to the product. Two first tests of 3 L each were filtered at 1500 rpm (˜375 g) and the liquid recovered. In a second step, 8 L were filtered in several parts at 3000 rpm (˜1500 g) to determine if further liquid extraction can be achieved. A filter of 1 μm porosity (model 3 54 FC) was chosen since it gave a reasonable liquid cross-flow. Also, this is the same filter used in previous filtration test with a 20% solution which gave good results. The EMBLICA used in these tests have same characteristics as described in Example 1.

Test 1

[0040] 3 L of a 33% solution of EMBLICA were filtered at a centrifuge speed of 1500 rpm. The filtration was slower than at 20% but almost complete after 15 min. The resulting filtrate solution constituting about ⅔ by weight of the original solution was opaque and about 70% initial material was recovered. In order to increase the recovery, a second test was made a higher centrifugation speed. No black particles were visually (macroscopically) observed in the filtrate but many were observed on the residue on the filter.

Test 2

[0041] 33% EMBLICA solution was filtered by using the same filter but a higher centrifugation speed of 3000 rpm. Filtration was only slightly improved despite a 4 times higher g force. Out of 12 kgs of initial material, only 8.3 kgs were obtained. No black particles were observed in the filtrate solution. Accordingly, filtration tests with a 33% w/w solution of EMBLICA show satisfactory elimination of black particles, similar to previous tests with 10 and 20% solutions. However, 33% weight concentration appears too high for maximal product throughput. Filtration at 18-22% is therefore preferred.

EXAMPLE 3

[0042] The solutions of Example 2 obtained by filtration at 1500 and 3000 rpm were spray dried separately. Conditions were an inlet temperature of 345±5° F., an outlet temperature of 230±5° F. and a feed rate of 100 ml/min. The spray drier was a 30 inch Bowen Lab unit.

[0043] The laboratory results were as follows:

[0044] Processed first:

[0045] 3000 rpm solution INPUT: 8.2 kgs OUTPUT: 1.395 kgs (+1.2 kgs) followed by

[0046] 1500 rpm solution INPUT: 3.7 kgs OUTPUT: 1.06 kgs (+0.37 kgs)

[0047] The OUTPUT weights correspond to the direct product obtained as well as the weight of sticking product brushed off the vessel's walls. The latter product caused by hot steel walls of the vessel shows a clearly darker color (orangish-brownish) than the direct dried product (off-white to light beige). To overcome such sticking it is contemplated that production vessels will include an additional insulation of the walls which will reduce, if not eliminate, this effect. No significant loss of material occurs during the spray drying process. The resulting product powder is quite dry, fluffy and slightly whiter than the original.

[0048] The highest product loss occurred during the centrifuge filtration step due to the high initial concentration in the test. A much higher filtration throughput can be obtained by using a 20% /w. solution.

[0049] The following table provides a chromatographic analysis of 2 lots.

Emblica ™ (Centrifuge-Spray dried sample):
Calculation of actives from HPLC data
1%⁢ ⁢small⁢ ⁢tannoids=∑ ⁢areas⁢ ⁢of⁢ ⁢active⁢ ⁢peaksTotal⁢ ⁢area⁢ ⁢of⁢ ⁢the⁢ ⁢chromatogram
Lot No. F15
Areas for the actives: Emblicanin A + Emblicanin B + Punigluconin +
Pedunculagin =
Areas of peaks 1, 3, 6, 8 = 894.95 + 513.28 + 261.87 +
891.97 = 2,562.07
Total area per HPLC: 2,929.93
% of actives = 2,562.07/2,929.93 = 87.45%
% of Emblicanin A = 894.95/2,929.93 = 30.55%
% of Emblicanin B = 513.28/2,929.93 = 17.52%
% of Punigluconon = 261.87/2,929.93 = 8.95%
% of Pedunculagin = 891.97/2,929.93 × 83.80 = 30.44%
Lot No. F30
Areas for the actives; Emblicanin A + Emblicanan B + Punigluconin +
Pedunculagin + Areas of peaks 1, 3, 6, 8 = 904.51 + 502.66 +
251.66 + 889.70 = 2,548.53
Total area per HPLC: 2,995.03
% of actives = 2,548.53/2,995.03 = 85.10%
% of Emblicanin A = 904.51/2,995.03 = 30.20%
% of Emblicanin B = 502.66/2,995.03 = 16.79%
% of Punigluconon = 251.66/2,995.03 = 8.40%
% of Pedunculagin = 889.70/2,995.03 = 29.70%

EXAMPLE 4

[0050] A 20% by weight of an aqueous dispersion of EMBLICA powder (100 Kg) was prepared by mixing the EMBLICA in water in a stainless-steel vessel filled with a mechanical agitator for about 1 hr in order to obtain an uniform dispersion. Then about 5 Kg of a diatomite filter aid (Celpure 1,000) was blended well to bind oligomeric/polymeric tannins. The slurry was mixed for approximately 30 min at room temperature. The residue was removed by centrifugation (i.e., in a Beckman™ J6B swinging one liter bucket rotor at 3000 rpm for 5 min), or by pressure filtering (i.e., through a coarse cellulose Cuno™. CPX-01A depth filter pad, with a pressure of 5 psi, 35 kPa). The filtered aqueous solution was then dried either by using a freeze drier or a spray drier.

EXAMPLE 5
Skin Care Lotion
	TRADE
INCI NAME	NAME/MANUFACTURER	% w/w
Phase A
Water (demineralized)		65.97
Disodium EDTA		0.10
Propylene Glycol		2.00
Sorbitol	Sorbo (70% soln.)/Uniqema	2.00
Sodium Lauryl Sulfate	Stepanol ME-Dry/Stepan	0.15
Phase B
Glyceryl stearate	Tegin M/Goldschmidt	5.00
Stearic acid	Emersol 132/Cognis	1.00
Persea Gratissima (Avocado) oil	Crodarom Avocadin/Croda	15.00
Unsaponifiables
Beeswax	White Bleached NF Beeswax	1.50
	Prills/Ross
Phase C
Water (demineralized)		5.00
Phyllanthus emblica fruit extract	Present Invention*	1.00
Phase D
Triethanolamine	TEA 99%/Union Carbide	0.28
Phase E
Propylene glycol, DMDM	Paragon/Mc Intyre	1.00
Hydantoin, Methylparaben
Total		100.00
Procedure: Combine A and heat to 70-75° C. Combine B and heat to 70-75° C. Add B to A while stirring. Add phase C at 30° C. Adjust pH to 5.0-6.0 with phase D. Add phase E. Mix until uniform.
*By “Present Invention” is meant the enriched EMBLICA having a decreased concentration of black specks and oligomer/polymers.

[0051]

EXAMPLE 6
Skin Lightening Lotion
	TRADE
INCI NAME	NAME/MANUFACTURER	% w/w
Phase A-1
Water (demineralized)		56.18
Disodium EDTA		0.05
Propylene Glycol		5.00
Phase A-2
Xantham Gum	Vanzan NF/Vanderbilt	0.25
Magnesium aluminum stearate	Veegum Ultra	0.40
	granules/Vanderbilt
Phase B
Cetearyl alcohol and cetearyl	Montanov 68/Seppic	7.00
glucoside
Apricot kernel oil	Lipovol P/Lipo	10.00
Octyl stearate	Cetiol 868/Cognis	3.00
Dimethicone	Dow Corning 200 Fluid	6.00
	10cst/Dow Corning
Phase C
Water (demineralized)		10.00
Phyllanthus emblica fruit extract	Present Invention	1.00
Phase D
Triethanolamine	TEA 99%/Union Carbide	0.12
Phase E
Phenoxyethanol,	Liquapar PE/Sutton	1.00
Isopropylparaben,
Isobutylparaben, Butylparaben
Total		100.00
Procedure: Disperse A-2 in A-1 and heat to 70-75° C. Combine B and heat to 70-75° C. Add B to A while stirring. Homogenize until mixture cools to 60° C. At 30° C. add phase C. Adjust pH with TEA to 4.0-5.0. Add phase E. Mix until uniform.

[0052]

EXAMPLE 7
Skin Lightening Lotion
	TRADE
INCI NAME	NAME/MANUFACTURER	% w/w
Phase A-1
Water (demineralized)		55.05
Disodium EDTA		0.05
Propylene Glycol		5.00
Phase A-2
Xantham Gum	Vanzan NF/Vanderbilt	0.25
Magnesium aluminum stearate	Veegum Ultra	0.40
	granules/Vanderbilt
Phase B
Cetearyl alcohol and cetearyl	Montanov 68/Seppic	7.00
glucoside
Apricot kernel oil	Lipovol P/Lipo	10.00
Octyl stearate	Cetiol 868/Cognis	3.00
Dimethicone	Dow Corning 200 Fluid	6.00
	10cst/Dow Corning
Phase C
Water (demineralized)		10.00
Phyllanthus emblica fruit extract	Present Invention	2.00
Phase D
Triethanolamine	TEA 99%/Union Carbide	0.25
Phase E
Phenoxyethanol,	Liquapar PE/Sutton	1.00
Isopropylparaben,
Isobutylparaben, Butylparaben
Total		100.00
Procedure: Disperse A-2 in A-1 and heat to 70-75° C. Combine B and heat to 70-75° C. Add B to A while stirring. Homogenize until mixture cools to 60° C. At 30° C. add phase C. Adjust pH with TEA to 4.0-5.0. Add phase E. Mix until uniform.

[0053]

EXAMPLE 8
Age-Defying Lotion
	TRADE
INCI NAME	NAME/MANUFACTURER	% w/w
Phase A-1
Water (demineralized)		59.15
Disodium EDTA		0.05
Propylene Glycol		5.00
Phase A-2
Xantham Gum	Vanzan NF/Vanderbilt	0.20
Phase B
PEG-6 stearate, ceteth-20,	Tefose 2561/Gattefosse	10.00
glyceryl
stearate, steareth-20, stearic acid
Stearic Acid	Emersol 132/Cognis	1.00
Hydrogenated castor oil	Cutina HR/Cognis	1.00
Octyldodecyl myristate	M.O.D./Gattefosse	8.00
Dimethicone	Dow Corning 200, 50cst/Dow	4.00
	Corning
Phenyltrimethicone	Dow Corning 556 Wax/Dow	2.00
	Coning
Sweet Almond oil	Cropure Almond/Croda	3.00
Phase C
Water (demineralized)		5.00
Phyllanthus emblica fruit extract	Present Invention	0.50
Phase D
Triethanolamine	TEA 99%/Union Carbide	0.10
Phase E
Phenoxyethanol,	Liquapar PE/Sutton	1.00
Isopropylparaben,
Isobutylparaben, Butylparaben
Total		100.00
Procedure: Disperse A-2 in A-1 and heat to 70-75° C. Combine B and heat to 70-75° C. Add B to A while stirring. Homogenize until mixture cools to 60° C. At 30° C. add phase C. Adjust pH with TEA to 5.0-6.0. Add phase E. Mix until uniform.

[0054]

EXAMPLE 9
Sunscreen Lotion
	TRADE
INCI NAME	NAME/MANUFACTURER	% w/w
Phase A
Butylmethoxydibenzoylmethane	Eusolex 9020/Rona	1.00
Glyceryl Stearate, Ceteareth-15	Tegocare 215, Pellets/Degussa	3.00
Decyl oleate	Cetiol V/Cognis	5.00
Isopropyl palmitate	Isopropyl palmitate	5.00
Dimethicone	Mlrasil DM 350	0.50
Stearyl alcohol	Lanette 18	2.00
Carbomer	Carbopol ETD 2050	0.10
Phase B
Glycerin	Glycerol (about 87%)	3.00
Ectoin	RonaCare Ectoin/Rona	0.50
Phenoxyethanol,	Liquapar PE/Sutton	1.00
Isopropylparaben,
Isobutylparaben, Butylparaben
Aqua (water), Ethyhexyl		15.00
metoxycinnamte, Silica, PVP,
Chlorphenesin, BHT
Water, demineralized	Aqua (water)	qs
Phase C
Phyllanthus emblica fruit extract	Present Invention	0.50
Phase D
Sodium hydroxide	Sodium hydroxide, 10%	0.45
	solution
Phase E
Perfume	Fragrance delicat/Drom	0.20
Total		100.00
Procedure: Heat phases A and B separately to 80° C. stir phase A. Homogenize. At 30° C., add phase C. Adjust pH with sodium hydroxide to 5.5. Finally add phase E to the emulsion.

[0055]

EXAMPLE 10
ANHYDROUS OIL-FREE GEL
INCI NAME	TRADE NAME/MANUFACTURER	% w/w
Phase A
Ozokerite	White Ozokerite SP-1020/Strahl &	3.00
	Pitsch
Cyclomethicone	Dow Corning 345 Fluid/Dow Corning	25.00
Cyclomethicone (and)	Gransil GCM/Grant Industries	60.00
Polysilicone-11
Phase B
Bismuth Oxychloride	Biron ® LF-2000/Rona	2.00
Phase C
Cyclomethicone	Dow Corning 345 Fluid/Dow Corning	3.60
Cyclomethicone (and)	Dow Corning 9040 Silicone	5.40
Dimethicone	Elastomer Blend/Dow Corning
Crosspolymer
Present Invention		1.00
Total		100.00
Procedure: Blend ingredients in Phase A; heat with mixing until clear and uniform. Add bismuth oxychoride and disperse with mixing. Blend ingredients in Phase C separately; the mixture should be smooth and contain no lumps. Cool Phase A/B to 50-60° C. and add Phase C with mixing. When
# the mixture is uniform it may be packaged.

[0056]

EXAMPLE 11
Capsules & Tablets
Ingredients	Composition (w/w, in %)	Quantity per tablet (mg)
1. Present invention	60.0	250
2. Avicel pH101	20.0	84.0
3. Starch 15000	17.5	75.5
4. Stearic acid, NF	2.0	8.5
(powder)
5. Cab-O-Sil	0.5	2.0
Procedure: 1 is granulated with starch paste to make it a free flowing powder. Blend all the ingredients, except 4, for 25 min. in a blender. Screen in 4 and blend for an additional 5 min. Compress into tablets using 7/16 in standard concave tooling. Alternately, the blended material can be
# filled into appropriate capsules.

[0057] Notwithstanding the details of the preceding embodiments, it is to be understood there are several broad concepts in the present invention.

[0058] The first broad concept relates to the treatment of a raw extract from Emblica officinalis. Once it is known that it is important to adjust the time, and/or temperature, and/or atmosphere and/or chemistry of the conditions of the extraction as to inhibit the formation of polymeric tannins and/or black specks, a chemical engineer or the like would be able to adjust such variables so as to inhibit the formation of the undesired components. This would require measuring the extent of the undesired components without adjustment of the variables and then adjusting the variables so as to provide an improved process. For example, lower temperatures and shorter residence times should result in a lower degree of oligomerization or polymerization. Likewise, the less oxygen in the atmosphere, the less likelihood of oxidation to form undesired impurities. Consequently, by adjusting at least one of the variables, it is possible that only one variable need be adjusted in order to obtain the desired inhibition, for example, temperature. Nevertheless, it is also contemplated that two or more variables may also be adjusted so as to arrive at the optimum conditions.

[0059] Another basic concept of the invention relates to concentrating the extract, e.g. in order to form a powder. Again, the temperature, time and atmosphere in which the concentrating is conducted will have an effect on the degree of impurities in the resultant dried composition. Consequently, a chemical engineer or the like will be able to adjust at least one of the variables in order to obtain a product which is substantially to completely devoid of black particles when viewed visually (macroscopically), preferably at least 95%, more preferably at least 99%). By “substantially devoid” is meant that the black particles are decreased in number compared to the number of black particles which would be present in the absence of the adjustment of the variables. Preferably, the composition should be completely devoid of black specks) but it is contemplated that it would be sufficient for esthetic purposes for the composition to contain not more than 100, preferably below 10 black specks per 500 grams of composition).

[0060] Another concept of the invention relates to the reduction of potentially biologically adverse components in the extract. This is accomplished, for example, by removing at least a portion of polymeric tannins having a molecular weight of above 1,000, and especially above 3000.

[0061] Thus, taking into consideration the various concepts and aspects of the invention, the preceding examples can be repeated with substantially similar success by substituting generically or specifically described steps and/or operating conditions for those set forth in the examples.

[0062] The entire disclosure of all applications, patents, and publications cited above, including those references set forth in said applications, patents and publications are hereby incorporated by reference.

[0063] From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.

Claims

1. In an extraction process comprising extracting a raw extract from Emblica officinalis the improvement comprising conducting the extraction under conditions of time, temperature and atmosphere, to inhibit the formation of black specks and/or oligomeric and/or polymeric tannins and/or oxidation products thereof.

2. A process according to claim 1, comprising inhibiting the formation of said oilgomeric and/or polymeric tannins having a molecular weight above 1000.

3. In a process of producing a powdered extract of Emblica officinalis, comprising the step of drying an aqueous solution of the extract, the improvement comprising conducting the drying under conditions of time, temperature and atmosphere so as to inhibit the formation of oligomeric and/or polymeric tannins and/or oxidation products thereof and/or black specks.

4. A process according to claim 3 comprising inhibiting the formation of said oligomeric and/or polymeric tannins having a molecular weight above 1000.

5. A process comprising enriching an extract of Emblica officinalis, comprising the steps of: A) providing an aqueous suspension of Emblica officinalis, said aqueous suspension containing dissolved components of Emblica officinalis and water-insoluble components comprising black specks and/or oligomeric and polymeric tannins; and B) separating the insoluble components from said dissolved components to obtain an enriched aqueous extract of Emblica officinalis.

6. A process according to claim 5, further comprising a preceding step of dispersing a powdered extract of Emblica officinalis in an aqueous solution to form said aqueous suspension.

7. A process according to claim 5, wherein said separating comprises subjecting said suspension to centrifugation or pressure filtration.

8. A process according to claim 5, wherein said separating comprises adding a filter-aid to said aqueous suspension and filtering out the insoluble components of the suspension so as to obtain an enriched aqueous filtrate of Emblica officinalis.

9. A process according to claim 5, wherein said aqueous suspension has a concentration of 5-30% by weight of total solids of Emblica officinalis.

10. A process according to claim 5, wherein said aqueous suspension has a concentration of 18-22% by weight of total solids of Emblica officinalis.

11. A process according to claim 6, wherein said aqueous suspension has a concentration of 5-30% by weight of total solids of Emblica officinalis.

12. A process according to claim 6, wherein said aqueous suspension has a concentration of 18-22% by weight of total solids of Emblica officinalis.

13. A process according to claim 10, comprising subjecting said aqueous suspension to sufficient centrifugation to obtain an enriched extract of Emblica officinalis macroscopically substantially to completely devoid of black specks.

14. A process according to claim 5, further comprising drying the separated enriched aqueous extract of Emblica officinalis.

15. A process according to claim 6, further comprising drying the separated enriched aqueous extract of Emblica officinalis.

16. A process according to claim 15, wherein said drying step comprises spray drying or freeze drying.

17. A process according to claim 14, comprising drying said solution of Emblica officinalis under conditions of time, temperature and atmosphere so as to inhibit the formation of oligomeric and/or polymeric tannins having a molecular weight of over 1000.

18. A process according to claim 16, wherein said drying comprises freeze drying.

19. An extract of Emblica officinalis produced by the process of claim 1.

20. An extract of Emblica officinalis produced by the process of claim 3.

21. An extract of Emblica officinalis produced by the process of claim 5.

22. An extract of Emblica officinalis produced by the process of claim 6.

23. In a powdered composition of Emblica officinalis, the improvement wherein said composition is macroscopically substantially to completely devoid of black specks.

24. A composition according to claim 23, wherein such composition contains at least 75% by weight of bio-active low molecular weight hydrolysable tannins.

25. In a powdered composition of, Emblica officinalis the improvement wherein the composition contains less than 5% by weight of oligomeric and polymeric tannins having a molecular weight of above 1000.

26. In a powdered composition of, Emblica officinalis, according to claim 23, the improvement wherein the composition contains less than 5% by weight of oligomeric and polymeric tannins having a molecular weight of above 3000.

27. A skin or hair or personal care composition formed from ingredients comprising a powdered composition according to claim 26.

28. A process according to claim 1, wherein the extraction is conducted so as to result in a water-soluble extract containing less than 5% by weight of oligomeric and polymeric tannins having a molecular weight of above 3,000.

29. A process according to claim 3, conducted under conditions sufficient to provide in a dried composition containing less than 5% by weight of oligomeric and polymeric tannins having a molecular weight of above 3,000 and substantially to completely devoid of black specks.

30. An extract produced in accordance with the process of claim 28.

31. A dried composition produced in accordance with the process of claim 29.

32. A skin or personal care composition according to claim 26 in the form of a lotion, crème, stick, spry or gel.

33. A skin or personal care composition according to claim 32 which contains about 0.05 to 5% of said tannins.

34. A pharmaceutical or nutritional composition formed from ingredients comprising a powdered composition according to claim 26 in the form of a tablet, capsules, elixir, syrup, or drinks.

35. A pharmaceutical or nutritional composition according to claim 34 formed from about 0.05 to 20% of said powdered composition.