RU2195919C2 - Substance for parodontium sickness treatment - Google Patents

Abstract

FIELD: medicine, stomatology. SUBSTANCE: substance for treatment of parodontium sickness comprises sage aqueous extract, vegetable raw oily extract, polyacrylate, distilled monoglycerides, triethanolamine, Trilon B, higher saturated alcohols, cosmetic stearin, 1,2-propylene glycol, nipagine, peppermint oil, alpha-tocopherol acetate, coniferous provitamin concentrate, soybean oil and purified water. Components are taken in the definite quantitative ratio. Substance allows to reduce treatment time and due to its consistence it retains prolonged contact with parodontium tissues. EFFECT: improved method of treatment, valuable medicinal properties of substance. 1 cl, 2 tbl

Description

 The invention relates to medicine, in particular to medicines in the field of dentistry, and can be used to treat periodontal disease.

 Known substance for the treatment of periodontal disease containing extracts of herbal medicines (A.I. Marchenko, A.I. Baranyuk "Medicinal plants in dentistry", 1981, Chisinau, pp. 25-36).

 The disadvantage of these funds is the low treatment effectiveness associated with the one-sided impact on the disease process, and the high duration of treatment.

 There is a method of treating periodontal diseases by prescribing oral baths using extracts of herbal medicines (P. I. Roshchina, L. N. Maksimovskaya "Medicines. Dentistry. 1989, Moscow, pp. 75-76).

 A disadvantage of the known methods is the low effectiveness of treatment associated with the rapid loss of activity of drugs due to the constant exposure to saliva and a significant duration of treatment.

 The purpose of the invention: to increase efficiency and reduce the duration of treatment.

The goal is achieved by the fact that produce a substance containing an aqueous extract of herbal preparations, and its composition includes (in percent):
- vegetable oil extract (1:10) - 0.50-1.00
- water extract of sage (1:10) - 8.00-10.00
- polyacrylate - 0.50-1.00
- triethanolamine - 0.20-0.30
- 1,2-propylene glycol - 3.00-4.00
- nipagin - 0.20-0.30
- Trilon B - 0.01-0.02
- distilled monoglycerides - 0.50-1.00
- higher fatty alcohols - 0.50-1.00
- cosmetic stearin - 0.50-1.00
- peppermint oil - 0.15-0.30
- alpha-tocopherol acetate - 0.15-0.20
- Coniferous provitamin concentrate - 2.00-3.00
- soybean oil - 3.00-4.00
- purified water - up to 100
and for the treatment of periodontal disease, it is placed in the affected area, and is separated from the effects of saliva, for example, by placing in an individually made mouthguard.

The substance is made as follows. In a 90 ml volume of water extract of sage (1: 10), 4 ml of an oil extract of a medicinal plant material, 1 ml of polyacrylate (the cross-linked polymer of Mars polyacrylic acid), 0.2 ml of triethanolamine, 3 ml of 1,2-propylene glycol, 0, 3 ml nipagin, 0.2 ml Trilon B, 1 ml monoglycerides, 1 ml higher fatty alcohols, up to 1 ml cosmetic stearin, 0.2 ml peppermint oil, 0.1 ml alpha-tocopherol acetate, 3 ml softwood softener concentrate, 3 ml of soybean oil, mix thoroughly until a homogeneous mass is obtained and placed inside a container with a temperature 8 ^o C. Before use, 865 ml of purified water is added to the container with the obtained substance. The resulting mixture is thoroughly mixed until a homogeneous mass and packaged.

 In the treatment of periodontal disease, the substance is placed in an individually made mouthguard, which is located in the affected area.

 In the table. Figures 1 and 2 show the prevalence of periodontal disease at a young age and in adults. Epidemiological studies of schoolchildren in Italy aged 8 to 12 years showed the presence of periodontal lesions in 97% (I. Angelo, G. Cjssard, 1971). According to K. Jacson (1975), Murray J. (1974) in England and the United States under the age of 17 years, gingivitis occurs in 36-90% of cases. B. Kowalcki (1974) and A. Semeruk-Mazurkiewier (1974) found gingivitis in 30.42 and 65% of Polish students, respectively. In the USA, 60% of adolescents suffer from periodontal disease (Gueen G., 1972). N. Miihlemann and A. Masor, having examined more than 1000 Zurich schoolchildren aged 7 to 17 years, found inflammatory changes in the gums in 80%.

 Patient I., 42 years old (control group) (see table. 3 at the end of the description).

 Diagnosis: chronic generalized periodontitis of moderate severity.

 In the process of treatment, a circular flap operation on the upper and lower jaw was performed with gingivoplasty, as well as the introduction of hydroxylapatite and honsuride into the bone pockets.

 In the postoperative period, the oral cavity was irrigated with chamomile solutions 3 times a day for 10 days, oral baths with chamomile solutions 3 times a day for 10 days.

Recommended by:
- 2 times a day (in the morning - after breakfast, in the evening - at bedtime), brush your teeth with a toothbrush and toothpaste for 5 minutes;
- repeat oral irrigation with the same solution, as well as conduct oral baths;
- after each meal, rinse your mouth actively for 3 minutes.

1 month after treatment:
- Schiller-Pisarev test - weakly positive;
- hygiene index - 2 points;
- Kulazhenko test - 30 seconds;
- RMA index - 2 points;
- bleeding index - 0.1.

6 months after treatment:
- Schiller-Pisarev test - weakly positive;
- hygiene index - 3 points;
- Kulazhenko test - 25 seconds;
- RMA index - 3 points;
- bleeding index - 0.1.

12 months after surgery:
- Schiller-Pisarev test - weakly positive;
- hygiene index - 3 points;
- Kulazhenko test - 22 seconds;
- RMA index - 3 points;
- bleeding index - 0.1.

 Patient U., 44 years old (experimental group) (see table. 4 at the end of the description).

 Diagnosis: chronic generalized periodontitis of moderate severity.

 In the process of treatment, a circular flap operation on the upper and lower jaw was performed with gingivoplasty, as well as the introduction of hydroxylapatite and honsuride into the bone pockets.

In the postoperative period, an application was carried out containing an aqueous extract of herbal preparations, and its composition included (in percent):
- vegetable oil extract (1:10) - 0.50-1.00
- water extract of sage (1:10) - 8.00-10.00
- polyacrylate - 0.50-1.00
- triethanolamine - 0.20-0.30
- 1,2-propylene glycol - 3.00-4.00
- nipagin - 0.20-0.30
- Trilon B - 0.01-0.02
- distilled monoglycerides - 0.50-1.00
- higher fatty alcohols - 0.50-1.00
- cosmetic stearin - 0.50-1.00
- peppermint oil - 0.15-0.30
- alpha-tocopherol acetate - 0.15-0.20
- Coniferous provitamin concentrate - 2.00-3.00
- soybean oil - 3.00-4.00
- purified water - up to 100
and for the treatment of periodontal disease, it was placed in the affected area, and separated from the effects of saliva by placing in an individually made mouthguard. This manipulation was performed twice within 7 days.

Recommended by:
- 2 times a day (in the morning - after breakfast, in the evening - at bedtime), brush your teeth with a toothbrush and toothpaste for 5 minutes;
- Once a month for 7 days, using an individual mouthguard, repeat applications at home;
- after each meal, rinse your mouth actively for 3 minutes.

1 month after treatment:
- Schiller-Pisarev test is negative;
- hygiene index - 1 point;
- Kulazhenko test - 35 seconds;
- RMA index - 0 points;
- bleeding index - 0.

6 months after treatment:
- Schiller-Pisarev test is negative;
- hygiene index - 1 point;
- Kulazhenko test - 40 seconds;
- RMA index - 0 points;
- bleeding index - 0.

12 months after surgery:
- Schiller-Pisarev test is negative;
- hygiene index - 2 points;
- Kulazhenko test - 42 seconds;
- RMA index - 1 point;
- bleeding index - 0.

 Based on the results of these clinical examples, it follows that it is possible to improve efficiency and reduce treatment time by using the above composition of herbal preparations for application by placing it in an individually made mouthguard.

Claims (1)

A substance for the treatment of periodontal diseases containing sage extract, characterized in that it additionally contains polyacrylate, triethanolamine, 1,2-propylene glycol, nipagin, trilon B, distilled monoglycerides, higher fatty alcohols, cosmetic stearin, peppermint oil, alpha-tocopherol acetate, softwood provitamin concentrate, soybean oil and water in the following components, wt. %:
Sage water extract - 8.00-10.00
Oil extract of plant materials (1: 10) - 0.5-1.00
Polyacrylate - 0.5-1.00
Distilled monoglycerides - 0.5-1.00
Triethanolamine - 0.20-0.30
Trilon B - 0.01-0.02
Higher fatty alcohols - 0.50-1.00
Cosmetic stearin - 0.50-1.00
1,2-Propylene glycol - 3.00-4.00
Nipagin - 0.20-0.30
Peppermint Oil - 0.15-0.30
Alpha-Tocopherol Acetate - 0.15-0.20
Coniferous provitamin concentrate - 2.00-3.00
Soybean Oil - 3.00-4.00
Purified water - Up to 100

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