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Combination of medication for antivirus in use for eye region and preparation method

A technology of antiviral drugs and compositions, applied in drug combinations, antiviral agents, pharmaceutical formulations, etc., can solve the problems of poor controllability of preparation quality standards, difficulty in achieving uniform drug delivery, unstable gel state, etc., and achieve quality The effect of high standard controllability, maintaining effective drug concentration, and reducing dosing frequency

Inactive Publication Date: 2008-01-09
成都三明药物研究所
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

It is a gel in vitro, the gel state is unstable, and the quality control of the preparation is poor. The method of use is to apply a small amount to the lower conjunctival sac each time. Causes pollution during use, and because it is applied in the lower conjunctival sac, it is difficult to achieve uniform drug administration, resulting in inconstant dosage and uneven application, which is inconvenient to use and easy to cause waste

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] The preparation of embodiment 1 medicine of the present invention

[0024] Prescription: Ganciclovir: 0.1g; Carbomer 940: 0.40g; Hypromellose: 1.20g; Disodium hydrogen phosphate: 0.25g; Sodium dihydrogen phosphate: 0.50g; Sodium chloride: 0.5g 1. Ethylparaben: 0.03g; appropriate amount of sodium hydroxide to adjust the pH value to 6.5.

[0025] With above-mentioned formula by following preparation technology:

[0026] a. Dissolve disodium hydrogen phosphate, sodium dihydrogen phosphate and methyl cellulose in appropriate amount of water for injection to form a transparent solution.

[0027] b. Take carbomer and add it to an appropriate amount of water for injection to swell. After the swelling is complete, add it to the transparent solution in step a above, and keep stirring to form a transparent solution.

[0028] c. Add ethylparaben and sodium chloride to an appropriate amount of water for injection until completely dissolved, and stir evenly, then add to the transp...

Embodiment 2

[0031] The preparation of embodiment 2 medicines of the present invention

[0032]Prescription: Ganciclovir: 0.05g; Carbomer 940: 0.30g; Hypromellose: 2.20g; Disodium hydrogen phosphate: 0.25g; Sodium dihydrogen phosphate: 0.50g; Sodium chloride: 0.5g ;

[0033] Above-mentioned formula is prepared by the technique of embodiment 1.

Embodiment 3

[0034] The preparation of embodiment 3 pharmaceutical composition of the present invention

[0035] Prescription: Ganciclovir: 0.05g; Carbomer 940: 0.50g; Hypromellose 1.30g; Disodium hydrogen phosphate: 0.20g; Sodium dihydrogen phosphate: 0.60g; Sodium chloride: 0.5g; Dumiphen: 0.03g; appropriate amount of sodium hydroxide to adjust the pH to 6.0.

[0036] The above formula is prepared according to the preparation process of Example 1, filled after passing the inspection, and autoclaved for subsequent use.

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Abstract

The present invention provides a combination of medication and preparation method thereof, particularly, provides an antivirus in use for eye region and preparation method thereof. The combination of medication is antivirus in use for eye taking Ganciclovir, Carbomer, hydroxypropylmethyl cellulose, and common preparation accessories in sue for eye as material. The invention prepares eye drops with in-situ gelatinizing technology.

Description

technical field [0001] The invention relates to an antiviral drug composition for eyes, in particular to an ophthalmic sustained-release preparation containing ganciclovir and a preparation method thereof. Background technique [0002] At present, the two most commonly used dosage forms of drugs for the treatment of eye infections are: solution and ophthalmic ointment. Solution-type eye drops, the principle of action is: after dripping into the eyes, the drug will be delivered with the secretion of tears, which is characterized by uniform distribution, but due to the continuous secretion of tears in the conjunctival sac and rapid removal from the nasolacrimal duct, it will be in the conjunctiva. The intracapsular residence time is very short, so the intraocular bioavailability is very low. Frequent administration is required to maintain normal drug concentration, which brings great inconvenience to patients, and the increase in the number of administrations greatly increase...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K31/522A61K9/00A61P37/02A61P31/12
Inventor 阳向波谢炜
Owner 成都三明药物研究所
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