The formulation and method of stabilizing and protecting biomaterials under strict storage and use conditions, wherein the formulation refers to the biological and bioactive embedded materials in the protective glass matrix, including living bacteria. Item 1: compounds with biological active substance characteristics, at least one forming agent and at least two forming agents. Second requirement: the composition of the first requirement, because the composition is a dry glass composition, including a bioactive substance. Fourth requirement: the composition of the first requirement,It is characterized by bioactive substances including cell, microorganism, virus, cell culture, bacteria, sample bacteria, plant and soil sample bacteria, yeast, protein, recombinant protein, enzyme, peptide, hormone, vaccine, drug, antibacterial agent, vitamin, a vitamin Carotene, ore, microorganism, fungicide, herbicide, insecticide or sperm. ILO Convention No. 5: the composition of ILO Convention No. 1, which is characterized by the fact that the agent of the mould is selected from a multi bag groupCellulose carboximetil, pacina, alginato sodio, alogenico sales, hydropropil methylcellulose (HPMC),Methylcellulose, carrageenan, Guarani rubber, Arcadia rubber, xantano rubber, garofen rubber, quinine and its derivatives, modified starch and starch, cyclohexane, inulina, maltinulin, glucose and their mixtures. Item 6: the composition of item 1, which is characterized by the fact that the number of matrix generators varies from about 1% by weight to about 20% by weight. Item 8: the composition required in Item 1, which is characterized by: the preparation made of glass is: protein, such as bovine and human serum albumin, protein protein protein, jelly,Immunoglobulin, insulating soybean protein, wheat protein, skimmed milk powder, casein, serum protein, pea protein and any protein hydrolysis； carbohydrate containing monosaccharide (cereal, d-manosa, blood sucking agent, etc.)2. Disacard includ
