YY/T 0719.8-2019Ophthalmic optics - Contact lens care products - Part 8: Test method for detergent (English PDF)
眼科光学 接触镜护理产品 第8部分:清洁剂测定方法
This is a limited preview
Buy now to download the full PDF (21 pages)
Need quotation for your management?
Get a formal quotation for YY/T 0719.8-2019 in 30 minutes.
Issued by
NMPA
Level / Type
Industry · Recommended
Issue date
October 23, 2019
Implementation date
October 1, 2020
Scope
YY/T 0719.8-2019 is the English-translated version of 眼科光学 接触镜护理产品 第8部分:清洁剂测定方法.
YY/T 0719.8-2019 is the Chinese pharmaceutical industry standard that gives the method for determining poloxamer or polyoxyethylene hydrogenated castor oil, the surfactant active ingredients, in contact lens care products.
It is the eighth part of the YY/T 0719 series and sets out the reagents, the preparation of the sample and the standards, the chromatographic determination and the calculation of the content, so that the declared amount can be verified. Issued on 23 October 2019, it has applied since 1 October 2020.
Found what you need?
Document preview — YY/T 0719.8-2019
National Standard of the People's Republic of China
Issued by: National Medical Products Administration of the People's Republic of China
Contents
- Foreword3
- 1 Scope4
- 2 Normative references4
- 3 General rule4
- 4 Test method4
- 5 Test report8
- Annex A (informative) Typical liquid chromatogram of poloxamer10
1 Scope
This Part of YY/T 0719 specifies the test method to determine the content of Poloxamer or epoxy ethylene hydrogenated castor oil as active ingredient in contact lens care products (hereinafter referred to as care products).
This Part is applicable to care products that the active ingredient of the detergent is poloxamer or epoxy ethylene hydrogenated castor oil.
2 Normative references
The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies.
GB/T 6682, Water for analytical laboratory use - Specification and test methods
3 General rule
The test method specified in this Part shall be carried out at room temperature, that is, 10°C~30°C. Unless otherwise specified, all reagents used are analytical reagents. The experimental water shall meet the requirements for grade two water specified in GB/T 6682.
4 Test method
4.1 Poloxamer
4.1.1 Gel chromatography
4.1.1.1 Test principle
Poloxamer is a polyoxyethylene polyoxypropylene ether block copolymer. It is a class of polymer nonionic surfactants. The commonly used models in care products are poloxamer 188 and poloxamer 407. This method uses a
b) Column temperature: 30°C;
c) Refractive index detector, temperature is 30°C;
d) Mobile phase: sodium dihydrogen phosphate solution (0.02mol/L): acetonitrile=7:3;
e) Flow rate: 0.7mL/min;
f) Injection volume: 50µL.
4.1.1.7 Determination and result analysis
Respectively conduct analysis determination to standard solution and sample.
Establish standard working curve and regression equation. Calculate the content of poloxamer in the sample. See Annex A for typical chromatograms.
4.1.2 Ultraviolet-visible spectrophotometry
4.1.2.1 Test principle
According to the characteristic that hydroxypropyl methylcellulose has the ability to form a gel after heating in an aqueous solution, and then dissolve after cooling, pre-process the care solution to remove HPMC. Use ultraviolet-visible spectrophotometry that takes iodine-potassium iodide solution as the developer to determine the poloxamer content in nursing solution in the care solution.
4.1.2.2 Instruments and reagents
4.1.2.2.3 Instruments: UV-visible spectrophotometer, 1cm quartz cuvette; analytical balance with accuracy of 0.1mg.
4.1.2.2.1 Reagents: iodine, potassium iodide
4.1.2.2.2 Reference substance: poloxamer
4.1.2.3 Solution preparation
Poloxamer standard stock solution (0.1mg/mL): Accurately weigh 0.5g of poloxamer for reference that has been dried to constant weight, to the nearest of 0.1mg. Use pure water to conduct ultrasonic dissolution and set volume into a 50mL volumetric flask. Shake well. Then accurately pipette 1mLof the above solution to a 100mL volumetric flask. Use pure water to set volume to the scale. Shake well to obtain the solution.
Iodine-potassium iodide color developing solution: Weigh 2.0g of potassium iodide. Add an appropriate amount of water to make it dissolved. Then accurately add 1.0g of iodine to make it dissolved. Transfer to a 100mL analytical balance with accuracy of 0.1mg.
4.2.3 Solution preparation
Epoxyethylene hydrogenated castor oil standard stock solution (0.2mg/mL):
Weigh 0.1g of RH40 reference substance, to the nearest of 0.1mg. Use pure water to dissolve. Set volume to a 50mL volumetric flask. Shake well. Then accurately pipette 1mLof the above solution to a 10mL volumetric flask. Use pure water to set volume to the scale. Shake well to obtain 0.2mg/mL standard stock solution.
Iodine-potassium iodide color developing solution: Weigh 2.0g of potassium iodide. Add an appropriate amount of water to make it dissolved. Then accurately add 1.0g of iodine to make it dissolved. Transfer to a 100mL volumetric flask. Add water to dilute to the scale. Shake well to obtain the solution (this product shall be kept away from light).
4.2.4 Preparation of standard solution
Respectively pipette 1.0mL~3.0mL of epoxy ethylene hydrogenated castor oil standard stock solution to 10mL volumetric flasks. Set volume and shake well.
Add 0.25mL of mixed color developing solution. Shake well to obtain a series of standard solutions with a concentration of 20 x 10^-6~60 x 10^-6. At least 5 concentration points shall be selected. Use the same method and take pure water for blank.
4.2.5 Sample processing
Precisely pipette the right amount of sample. Dilute to a concentration about 40 x 10^-6. Then accurately add 0.25mL of iodine-potassium iodide color developing solution. Shake well.
4.2.6 Determination and result analysis
After standard and sample are placed for 2h, at 500nm, determine the absorbance. Perform parallel determination of 3 sets of data. Establish working standard curve and regression equation. Calculate the content of epoxy ethylene hydrogenated castor oil in the sample according to the standard curve.
5 Test report
The test report shall at least contain the following information:
a) Information about test sample;
b) Reference number to this Part; […]
......
This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 21 pages — is available in the English PDF.
Referenced standards
Normative references
Similar standards
How to Download YY/T 0719.8-2019
- 1
Add to cart
Click "Download PDF" on this page and choose "Buy this standard". You can add more standards before checkout.
- 2
Checkout
Enter your email and billing details. Payment is processed securely by Stripe (cards or bank transfer). Prefer bank details? Request a quotation (min. order $300).
- 3
Instant delivery (0–9 sec)
Delivery is automatic: within seconds of payment you'll receive an email with a secure download link. The link stays valid for 72 hours.
- 4
Invoice included
A tax invoice is attached to the confirmation email. Need a custom invoice? Contact us.
Related Standards
GB/T 6682-2008 — Water for analytical laboratory use - Specification and test methods
YY/T 0719.9-2021 — Ophthalmic optics - Contact lens care products - Part 9: Test method for chelator
YY/T 0719.6-2020 — Ophthalmic optics—Contact lens care products - Part 6: Guidelines for determination of shelf-life
Secure payment via Stripe
Payments accepted
YY/T 0719.8-2019
$165.00