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   Cinnamomum(Cinnamon) cassia.
 
 

Cinnamomun cassia


 English name: Cinnamon
   
 Family: Lauraceae
   
 Part used: Barks.
 
  Traditional uses :  
 
Cinnamon is one of the oldest medicines, mentioned in Chinese texts as long as 4000 years ago and Ayurvedic practioners used cinnamon to improve circulation and strenghten a weakened constitution1.
   
  Phytochemistry:
 
Cinnamon contains volatile oils (1–4%) of cinnamaldehyde (60–80%), eugenol (up to 10%) and trans-cinnamic acid (5–10%); phenolic compounds (4–10%), condensed tannins, catechins, proanthocyanidins, monoterpenes, sesquiterpenes (pinene), calcium-monoterpenes oxalate, gum, mucilage, resin, starch, sugars and traces of coumarin.
   
  Pharmacology:
 
Cinnamomum cassia has been reported to have an anti diabetic2-5, antimicrobial6-7, antibacterial8, antifungal9, antitumour10, immunomodulatory11, and anti-inflammatory activities12. In addition, it is found to be effective in the treatment of cancer13.
   
  Indication:
 
Blood sugar management and weight management.

  References:
   
1.
K. Toriizuka, Basic lecture of Kampo medicine: pharmacological effect of cinnamon, Kampo Med.
11 (1998) 431/ 436.
2.
Mang. B et al., Eur J Clin Invest, 2006: 36 (5): PP 340-344.
3.
Alam Khan et al., Diabetes Care, 2003: 26 (12): PP 3215-3218
4.
Mahpara Safdar et al., Pakistan Journal of Nutrition, 2004: 3 (5): PP 268-272.
5.
Sung HK et al. J Ethanopharmacol. 2006; 104; pp 119-123.
6.
Ooi LS and et al, “Antimicrobial Activities of Cinnamon Oil and Cinnamaldehyde from the Chinese
Medicinal Herb Cinnamomum cassia Blume”, Am J Chin Med. 2006; 34(3):511-22.
7.
Mau J, and et al “Antimicrobial effect of extracts from Chinese chive, cinnamon, and corni
fructus.” J Agric Food Chem, 2001; 49(1):183-8.
8.
Lee HS and Ahn YJ, “Growth-Inhibiting Effects of Cinnamomum cassia Bark-Derived Materials on
Human Intestinal Bacteria”, J Agric Food Chem., 1998 19;46(1):8-12.
9.
Giordani R,and et al, “ Potentiation of antifungal activity of amphotericin B by
essential oil from Cinnamomum cassia”, Phytother Res. 2006 Jan;20(1):58-61.

10.
Moon EY, and et al., “Delayed occurrence of H-ras12V-induced hepatocellular carcinoma with
long-term treatment with cinnamaldehydes”. Eur J Pharmacol. 2006, 20;530(3):270-5.
11.
Koh WSand et al., “Cinnamaldehyde inhibits lymphocyte proliferation and modulates T-cell
differentiation”, Int J Immunopharmacol.1998Nov; 20(11):643-60.
12.
Hong CH, “Evaluation of natural products on inhibition of inducible cyclooxygenase (COX-2) and
nitric oxide synthase (iNOS) in cultured mouse macrophage cells”, J Ethnopharmacol. 2002 Nov;83(1-2):153-9.
13.
Shan BE, and et al., “Stimulating activity of Chinese medicinal herbs on human lymphocytes in
vitro”, Int J Immunopharmacol. 1999; 21(3):149-59.
   

 DOC NO. :  NR/QCD/SPC/136
 ISSUE DATE :  02-04-2007
 REVISION NO. :  00
   ANALYTICAL SPECIFICATION  NUMBER OF PAGES :  01
TITLE : CINNAMOMUM CASSIA EXTRACT (³10% TOTAL POLYPHENOLS)
   Plant part :  Bark
   Fresh/Dry
:  Dry

Sl. No.

Tests

Limits

Protocol

1.      

Description

Reddish brown to Dark brown powder.

2.      

Identification

To pass the test

By HPLC

3.      

Physico-chemical analysis

< 8.0

As per USP <921> Method II

Moisture (%w/w)

Ash content (%w/w)

< 15.0

 

As per USP<561>

Acid insoluble Ash (%w/w)

< 5.0

Total soluble solids (%w/w)

> 90.0

pH of 5% w/v solution

4.0 - 7.0

As per USP<791>

4.      

Particle Size

0.15 - 0.60

As per USP <616> Method - I

Bulk Density (g/cc)

Tapped bulk density (g/cc)

0.20 - 0.80

Material passing through 30# BS/35 ASTM (%w/w)

> 99.0

As per USP <786> Particle Size distribution.

5.      

Heavy metal analysis

< 10 ppm

AAS / ICP -ES

Lead

Arsenic

< 2 ppm

Cadmium

< 1 ppm

Mercury

< 0.1 ppm

6.      

Microbiological analysis

< 104 cfu g-1

As per WHO/PHARMA/92.559/Rev.1 Pg.49-52 / As per USP <61> & <62>

As per FIP Guidelines

Total Viable Aerobic Count

Total Enterobacteriaceae

< 102 org g-1

Total Fungal Count

< 102 fs g-1

7.      

Test for Specific Pathogen

Absent

As per FIP Guidelines

E.coli (1g)

Salmonella Sp. (10g)

Absent

S.aureus (1g)

Absent

8.      

Mycotoxin analysis

< 5 ppb

As per USP

Aflatoxins (B1 + B2 + G1 + G2)

9.      

Residual solvent analysis

< 3000

As per USP

As per ICH Guidelines

Methanol (ppm)

10.  

Pesticide residue analysis

To comply with USP

As per AOAC / USP

As per USP & BP Limits

Organochlorine Pesticides

Organophosphorus Pesticides

Synthetic pyrethroids

11.  

Coumarin content

 

 

Coumarin content (ppm)

< 100.0

By HPLC

12.  

Bio-Assay

 

 

a-amylase Inhibition IC50 (mcg/ml)                      

< 100.0

[NR/BSY/SOP/004/002]

13.  

Phytochemical analysis

³ 10.0

By Spectrophotometry

Total Polyphenols (%w/w)



 
 
             
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