Evaluation of secretory mucin concentration of patients with squamous cell carcinoma oral cavity.

Purpose: Secretory salivary mucins constitute a heterogenous group of glycoproteins, synthesized and secreted by submandibular, sublingual gland and small glands of oral mucosa. The most significant functions of mucins in case of oral cavity carcinoma are: participation in oral pellicle formation, lubrication and creation of heterotypic complexing. The aim of this study was to assess mucins concentration, and finally to establish the correlation between concentration of mucins in saliva and clinical advancement according to TNM.

[Oral cavity health status among dentistry students in the Medical University of Bialystok].

The aim of this study was to analyse oral cavity hygiene, general health status and health behaviour of students studying on the last two years on the faculty of dentistry in the Medical University of Bialystok. 127 students were examined: 48 (37.8%) from the fourth and 79 (62.

Salivary epidermal growth factor in oral cavity cancer.

Salivary epidermal growth factor (EGF) effect on oral cancer biology is unknown. We examined changes in minute volumes of whole resting and stimulated saliva, EGF concentration and its output (ELISA) in whole resting and stimulated saliva before and 2 weeks after surgical treatment in oral carcinoma patients compared to the control group. After stimulation salivary flow increased both in the control (P=0.

[House fly development after chitin biosynthesis inhibitor application to eggs].

Nine asymmetrically substituted ureas were bioassayed against house-fly (Musca domestica L.) eggs. The compounds included benzoylaryl urea derivatives, shown in Table I, (compounds 1 and 3-8) and benzoylheteroaryl ureas (2 and 9) which previously revealed effective inhibition of metamorphosis and reproduction when applied in food to the larvae and adults.

[Effect of selected compounds from the group of chitin synthesis inhibitors on insects of sanitary importance].

The effect of three aryl and heteroaryl dichlorobenzoylurea compounds as insect chitin inhibitors on sanitary important insects were investigated. These compounds were given insects: larvae and adults flies (Musca domestica) and cockroaches (Blattella germanica) with food. The best results on flies were after exposition to AG-6 and on cockroaches to AG-5.

[Effectiveness of 2,6-dihalogenbenzoyl urea derivatives as potential inhibitors of chitin biosynthesis regarding the house fly Musca domestica L. and cockroach Blatella germanica L].

The biological activity was determined of 20 compounds from the group of asymmetrically substituted urea derivatives. They were derivatives of 1-(hetero)-aryl-3(2,6-dichlorobenzoyl)urea, compounds in Table 1, (1-12) which represented three groups of compounds: a) monochlorine or trifluoromethyl derivatives of benzene, b) monomethyl-substituted 2-pyridine derivatives, c) a derivative of 5-bromo-3-pyridine, and symmetrical derivates (Table 2 compounds 1-8) 2.2; 3.

Antineoplastic activity of new linear hydrazine derivatives.

A series of hydrazine derivatives was tested for antineoplastic activity. Cyanoacetic acid hydrazide (I), cyanoacetic acid methylhydrazide (II) and N-thioamido-N'-cyano-acethylhydrazine (VI) appeared to be the most active agents against sarcoma 180, Ehrlich carcinoma and Nemeth Kellner lymphoma. The maximum tumor weight inhibition ranged from 70 to 90%.

Biological activity of 1,4-dihydropyridine derivatives.

Six new 1,4-dihydropyridine derivatives were evaluated in vitro for antimicrobial and cytotoxic effects and in vivo for antineoplastic activity. These compounds inhibited the growth of most of Gram-positive and Gram-negative bacteria at concentrations of 50 and 100 micrograms/ml. Concentrations effective against fungi were somewhat lower (25-50 micrograms/ml).