Picrorhiza kurrooa Root and Rhizome Powder

Picrorhiza Species Root and Rhizome Powder

Proposed For Development Version 0.1

Picrorhiza kurrooa Root and Rhizome Powder

 


 

DEFINITION

 

The article consists of the dried root and rhizome of Picrorhiza kurrooa Royle (Family Plantaginaceae), reduced to powder or very fine powder. It contains NLT 3.5% of iridoid glycosides calculated as the sum of picroside I and picroside II on the anhydrous basis.

 

POTENTIAL CONFOUNDING MATERIALS

Picrorhiza scrophulariiflora Pennell

 

CONSTITUENTS OF INTEREST

Iridoid glycosides: Picroside I and picroside II

 

IDENTIFICATION

• A. Botanical Characteristics

Dusty grey; shows group of fragments of cork cells, thick walled. parenchyma, pitted vessels and aseptate fibers, simple round to oval, starch grains, measuring 25-104 μm in diameter.

 

B. Thin-Layer Chromatography

Standard solution A: 0.5 mg/mL of USP Picroside I RS in methanol

Standard solution B: 80 mg/mL of USP Picrorhiza kurrooa Root and Rhizome Dry Extract RS in methanol

Sample solution: Sonicate 2 g of Picrorhiza kurrooa Root and Rhizome Powder in 25 mL methanol for 10 min, centrifuge, and use supernatant.

Chromatographic system

(See Chromatography <621>, Thin-Layer Chromatography.)

Adsorbent: Use a suitable chromatographic material with an average particle size of 5 µm (HPTLC plates)

Application volume: 10 µL of Standard solution A, 10 µL of Standard solution B, and 10 µL of Sample solution; as 10-mm bands

Relative Humidity: Condition the plate to a relative humidity of about 33% using a suitable device

Developing solvent system: Ethyl acetate, methanol, and water (82:10:0.8)

Developing distance: 6 cm

Derivatization reagent: Anisaldehyde-sulfuric acid reagent

Analysis

Samples: Standard solution A, Standard solution B, and Sample solution.

Apply the samples as bands to a suitable high performance thin-layer chromatographic plate and dry in air (see <621> Chromatography). Develop the chromatograms in a saturated chamber, remove the plate from the chamber, treat with Derivatization reagent, heat for 3 min at 100°. Examine under visible light.

System Suitability: Under the visible light, the chromatogram of Standard solution B exhibits in the lower half about seven dark brown bands with most intense two bands close to upper section of lower half; one with higher RF corresponding to the band due to Picroside I in the chromatogram of Standard solution A.

Acceptance criteria: Under the visible light, the chromatogram of the Sample solution exhibits a strong dark brown band in the middle of the chromatogram that corresponds to the band due to picroside I in the Chromatogram of Standard solution A. About seven dark brown bands, with second strong band with lower RF than picroside I which corresponds to picroside II, exhibit in the lower half of the chromatogram of the Sample solution.

  

C. HPLC

Analysis: Proceed as directed in the test for Content of Iridoid glycosides

  Acceptance criteria: The chromatogram of the Sample solution exhibits peaks at the retention times corresponding to the peaks due to picroside I and picroside II of Standard solution B

 

ASSAY

• Content of Iridoid Glycosides

Solution A: Dissolve 0.136 g of anhydrous potassium dihydrogen orthophosphate (KH2PO4) in 900 mL of water and add 0.5 mL of orthophosphoric acid. Make up to 1,000 mL with water.

Solution B: Acetonitrile 

Mobile phase: See Table 1.

 

Table 1

  

Time (min)

Solution A (%)

Solution B (%)

0

85

15

7

80

20

15

70

30

20

20

80

22

20

80

25

85

15

30

85

15

 

Standard solution A: 0.015 mg/mL of USP Picroside I RS in methanol

Standard solution B: 0.6 mg/mL USP Picrorhiza kurrooa Root and Rhizome Dry Extract RS in methanol, sonicate if necessary. Before injection, pass through a membrane filter of 0.45-μm or fine pore size. Discard the first few mL of the filtrate.

Sample solution: Transfer 0.5 g of Picrorhiza kurrooa Root and Rhizome Powder to a flask, add 50 mL methanol and reflux for 20 min. Repeat 4-5 times for exhaustive extraction. Combine each extract to adjust volume to 100 mL with methanol.  

Chromatographic system

(See <621> Chromatography, System Suitability.)

Detector: UV 263 nm

Column: 4.6-mm × 25-cm, 5-µm packing L1 (similar to Luna 5-µ C18 (2)-100A)

Flow rate: 1.5 mL/min

Injection volume: 20 µL

System suitability

Sample: Standard solution A and Standard solution B

Suitability requirements

Chromatogram similarity: The chromatogram from Standard solution B is similar to the reference chromatogram provided with the lot of USP Picrorhiza kurrooa Root and Rhizome Dry Extract RS being used.

Resolution: NLT 2.0 between picroside I and picroside II

Tailing factor: NMT 1.5

Relative standard deviation: NMT 2.5%

Analysis

Samples: Standard solution A, Standard solution B and Sample solution

Using the chromatogram of Standard solution A, Standard solution B, and the reference chromatogram provided with the lot of USP Picrorhiza kurrooa Root and Rhizome Dry Extract RS being used, identify the retention times of the peaks corresponding to picroside I and picroside II. The approximate relative retention times of the peaks for picroside I and picroside II are 1.00 and 0.77, respectively.

Calculate the percentage of Iridoid glycosides in the portion of Picrorhiza kurrooa Root and Rhizome Powder taken: 

 

Result = (rU/rS) × CS × (V/W) × F × 100

 

rU          = response from the Sample solution

rS          = response from the Standard solution A

CS         = concentration of the Standard solution A (mg/mL)

V          = volume of the Sample solution (mL)

W         = weight of Picrorhiza kurrooa Root and Rhizome Powder taken to prepare the Sample solution, (mg)

F          = conversion factor for the analyte; 1.0 for picroside I and 1.68 for picroside II

 

Acceptance criteria: NLT 3.5% on the anhydrous basis

 

CONTAMINANTS

• Elemental Impurities—Procedures <233>

Acceptance criteria

Arsenic: NMT 2.0 µg/g

Cadmium: NMT 0.5 µg/g

Lead: NMT 5.0 µg/g

Mercury: NMT 0.2 µg/g

• Articles of Botanical Origin, General Method for Pesticide Residues Analysis <561>: Meets the requirements

• Articles of Botanical Origin, Test for Aflatoxins <561>: Meets the requirements

• Microbial Enumeration Tests <61>: The total aerobic bacterial count does not exceed 105 cfu/g, the total combined molds and yeasts count does not exceed 103 cfu/g, and the bile-tolerant Gram-negative bacteria does not exceed 103 cfu/g.

• Tests for Specified Microorganisms <62>: Meets the requirements of the tests for the absence of Salmonella species and Escherichia coli

 

SPECIFIC TESTS

• Articles of Botanical Origin, Alcohol-Soluble Extractives, Method 1 <561>: NLT 10.0%

• Articles of Botanical Origin, Water-Soluble Extractives, Method 2 <561>: NLT 20.0%

• Articles of Botanical Origin, Total Ash <561>

Analysis: 2.0 g of Picrorhiza kurrooa Root and Rhizome Powder

Acceptance criteria: NMT 7%

• Articles of Botanical Origin, Acid-Insoluble Ash <561>

Analysis: 2.0 g of Picrorhiza kurrooa Root and Rhizome Powder

Acceptance criteria: NMT 1%

Water Determination, Method III <921>: NMT 10.0%

 

ADDITIONAL REQUIREMENTS

• Packaging and Storage: Preserve in well-closed containers, protected from light and moisture, and store at room temperature.

• Labeling: The label states the Latin binomial and the part(s) of the plant from which the article was obtained.

• USP Reference Standards <11>

USP Aflatoxins RS

USP Picrorhiza kurrooa Root and Rhizome Dry Extract RS

  USP Picroside I RS

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Proposed For Comment Version 0.2