Picrorhiza Species Root and Rhizome Powder

This article is compiled based on the United States Pharmacopeia (USP) – 2025 Edition

Issued and maintained by the United States Pharmacopeial Convention (USP)

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1 DEFINITION

Picrorhiza Species Root and Rhizome Powder consists of the dried root and rhizome of Picrorhiza kurroa Royle ex Benth. (Fam. Plantaginaceae) reduced to powder or very fine powder^.1 Picrorhiza Species Root and Rhizome Powder contains NLT 3.5% of iridoid glycosides, calculated as the sum of picroside I and picroside II on the anhydrous basis.

2 IDENTIFICATION

2.1 A. HPTLC for Articles of Botanical Origin 〈203〉

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

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

Sample solution: Sonicate 500 mg of Picrorhiza Species Root and Rhizome Powder, accurately weighed, in 5 mL of methanol for 15 min.

Centrifuge and use the supernatant.

2.1.1 Chromatographic system

(See standard parameters as defined in HPTLC for Articles of Botanical Origin 〈203〉, Table 1.)

Application volume: 2 µL each of Standard solution A, Standard solution B, and the Sample solution, as 8-mm bands Developing solvent system: 2-Butanone, isopropyl alcohol, and formic acid (90:10:5)

Derivatization reagent: Prepare the anisaldehyde–sulfuric acid reagent as follows. Add 20 mL of acetic acid and 10 mL of sulfuric acid to 170 mL of cold methanol and mix well. After cooling to room temperature, add 1 mL of anisaldehyde.

2.1.2 Analysis

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

Apply the Samples as bands to a suitable HPTLC plate and dry in air. Develop in a saturated chamber, remove the plate from the chamber, and dry. Treat with the Derivatization reagent, heat for 3 min at 100°, and examine under long-wave UV light and under white light. System suitability

Under long-wave UV light: Standard solution B exhibits about 5–6 blue or purple bands and/or yellow, brown, or green bands in the lower half section, with the band near the middle section (near R_F 0.45) corresponding to picroside I in Standard solution A. The intense blue fluorescent band at about R_F 0.25 corresponds to picroside II. Additional blue or purple and/or pink or green fluorescent bands are observed in the upper-half section.

Under white light: Standard solution B exhibits about 4–5 brown bands in the lower-half section, with the most intense band close to the upper-most section (near R_F 0.45) and corresponding in R_F and color to picroside I in Standard solution A. Another intense band (near R_F 0.25) corresponds to picroside II.

2.1.3 Acceptance criteria

Under long-wave UV light: The Sample solution exhibits a blue or purple fluorescent band and a yellow, brown, or green fluorescent band in the lower-half section (near R_F 0.45) corresponding in R_F and color to picroside I in Standard solution A. The most intense blue fluorescent band (near R_F 0.25) corresponds to picroside II. Additional blue or purple and/or pink or green fluorescent bands are observed in the upper-half section.

Under white light: The Sample solution exhibits about 4–5 brown bands in the lower-half section, with the most intense band close to the upper-most section (near R_F 0.45) and corresponding in R_F and color to picroside I in Standard solution A. Another intense band (near R_F 0.25) corresponds to picroside II.

2.2 B. HPLC

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

Acceptance criteria: The Sample solution exhibits the most intense peak at a retention time corresponding to picroside I in Standard solution A and Standard solution B. The second most intense peak is picroside II. Three additional peaks, two between picroside I and picroside II and one before picroside II, are observed.

3 COMPOSITION

Content of Iridoid Glycosides

Solution A: Dissolve 0.136 g of anhydrous potassium phosphate, monobasic in 900 mL of water, and add 0.5 mL of phosphoric acid. Dilute with water to 1000 mL.

Solution B: Acetonitrile

Mobile phase: See Table 1.

Table 1

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

Standard solution B: 0.6 mg/mL of USP Picrorhiza kurroa Root and Rhizome Dry Extract RS in methanol. Sonicate if necessary. Before injection, pass the solution through a suitable membrane filter of 0.45-µm or finer pore size. Discard the first few milliliters of the filtrate. Sample solution: Transfer 0.5 g of Picrorhiza Species Root and Rhizome Powder, accurately weighed, to a suitable flask. Add 50 mL of methanol and reflux for 20 min. Repeat 4–5 times for exhaustive extraction. Combine each extract and dilute with methanol to 100 mL. Before injection, pass the solution through a suitable membrane filter of 0.45-μm or finer pore size. Discard the first few milliliters of the filtrate.

3.1 Chromatographic system

(See Chromatography 〈621〉, System Suitability.)

Mode: LC

Detector: UV 263 nm

Column: 4.6-mm × 25-cm; 5-µm packing L1

Column temperature: 30°

Flow rate: 1.5 mL/min

Injection volume: 20 µL

3.2 System suitability

Samples: Standard solution A and Standard solution B

Suitability requirements

Resolution: NLT 1.5 between picroside I and picroside II, Standard solution B

Tailing factor: NMT 1.5 for picroside I, Standard solution A

Relative standard deviation: NMT 2.5% for picroside I in repeated injections, Standard solution A

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

3.3 Analysis

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

Using the chromatograms of Standard solution A and Standard solution B and the reference chromatogram provided with the lot of USP Picrorhiza kurroa 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 separately the percentages of picroside I and picroside II in the portion of Picrorhiza Species Root and Rhizome Powder taken:

Result = (r_U /r_S) × C_S × (V/W) × F × 100

r_U = peak area of picroside I or picroside II from the Sample solution

r_S = peak area of picroside I from Standard solution A

C_S = concentration of USP Picroside I RS in Standard solution A (mg/mL)

V = volume of the Sample solution (mL)

W = weight of Picrorhiza Species Root and Rhizome Powder used to prepare the Sample solution (mg)

F = conversion factor for the analyte (1.0 for picroside I, 1.74 for picroside II)

Calculate the content of iridoid glycosides as the sum of the percentages of picroside I and picroside II.

Acceptance criteria: NLT 3.5% on the anhydrous basis

4 CONTAMINANTS

Articles of Botanical Origin 〈561〉, Limits of Elemental Impurities: Meets the requirements

Articles of Botanical Origin 〈561〉, Pesticide Residue Analysis: Meets the requirements

Microbial Enumeration Tests 〈2021〉: 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 bacterial count does not exceed 103 cfu/g.

Absence of Specified Microorganisms 〈2022〉, Test Procedures, Test for Absence of Salmonella Species and Test for Absence of Escherichia coli: Meets the requirements

5 SPECIFIC TESTS

Botanical Characteristics: Dusty gray; groups of fragments of cork cells; thick-walled parenchyma; pitted vessels and aseptate bers; simple, round to oval starch grains measuring 25–104 µm in diameter.

Articles of Botanical Origin 〈561〉, Methods of Analysis, Foreign Organic Matter: NMT 2.0%

Articles of Botanical Origin 〈561〉, Methods of Analysis, Alcohol-Soluble Extractives, Method 1: NLT 10.0%

Articles of Botanical Origin 〈561〉, Methods of Analysis, Water-Soluble Extractives, Method 1: NLT 20.0%

Articles of Botanical Origin 〈561〉, Methods of Analysis, Total Ash: NMT 7.0%

Articles of Botanical Origin 〈561〉, Methods of Analysis, Acid-Insoluble Ash: NMT 1.0%

Water Determination 〈921〉, Method III

Sample: 2.0 g of Picrorhiza Species Root and Rhizome Powder

Analysis: Dry the Sample at 105° for 2 h.

Acceptance criteria: NMT 10%

6 ADDITIONAL REQUIREMENTS

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

Labeling: The label states the Latin binomial following the ocial name of the plant from which the article was derived.

USP Reference Standards 〈11〉

USP Picrorhiza kurroa Root and Rhizome Dry Extract RS

USP Picroside I RS (USP 1-May-2024)

¹ The synonym status of the species names Picrorhiza kurroa Royle ex Benth. and Picrorhiza kurrooa Royle is unresolved at this time.