| Identity, purity
and quality of aloe vera are determined by third-party laboratory
analysis using a proton nuclear magnetic resonance spectroscopy (1H-NMR)
method together with other traditional wet chemistry methods. Identification
is based upon polysaccharides which possess the 2,3,6 acetylation
pattern that is unique to aloe only. Quality is measured by the profile
of organic acids, some of which are native to aloe and others that
indicate possible microbial contamination or improper handling. Purity
is determined by the absence of foreign materials or presence of additives
or excipients such as preservatives, extenders, etc. - all of which
are detectable in the NMR spectral patterns. A product must be comparable
to native aloe gel or whole leaf in each of these three areas to achieve
certification. |
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Analytical Methods
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Criteria
|
Analytical Method
|
| Total Solids |
Total Solids |
| HPLC (Malic Acid) |
1H-NMR |
| Magnesium |
N/A |
| Calcium |
N/A |
| |
Size exclusion chromatography |
|
Freshness quality from 1H-NMR
includes:
- Malic acid (primary, native organic acid)
- Other organic acids such as lactate, succinate,
furnarate, formate and acetate are products of enzymatic or hydrolytic
degradation and should be absent or at very low concentration.
- Free glucose:mannose ratio > 2:1
- Presence of glucomannan
|
Composition Fingerprint from 1H-NMR includes:
- Glucomannan
- Free glucose as monosaccharide
- Malic Acid
- Bonded acetate
- C-acetylation pattern
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|