scholarly journals JENNERIAN PROPHYLAXIS BY MEANS OF INTRADERMAL INJECTIONS OF CULTURE VACCINE VIRUS

1935 ◽  
Vol 62 (4) ◽  
pp. 549-560 ◽  
Author(s):  
Thomas M. Rivers ◽  
S. M. Ward
Keyword(s):  
Saline Solution ◽  
Vaccine Virus ◽  
In Vitro Cultivation ◽  
Human Beings ◽  
Intradermal Vaccination ◽  
Immune Reactions ◽  
Gum Acacia ◽  
Culture Virus

The second revived strain of culture vaccine virus has been propagated through 130 culture passages during a period of 3 years. It seems to be adapted to in vitro cultivation and still has an intradermal titer (rabbits) of 1 to 100,000 or 1 to 1,000,000. Intradermal inoculations in human beings of 0.1 cc. amounts of culture virus diluted from 2.5 to 10 times result in primary takes in unvaccinated people and immune reactions or accelerated takes in individuals previously successfully vaccinated. Primary takes produce an immunity to standard strains of calf lymph. Culture virus mixed with purified gum acacia (2.5 per cent), frozen, desiccated, and sealed in vacuo retains its activity for a month at 37°C., and when the dried virus is resuspended in saline solution it is suitable for intradermal vaccination of human beings.

scholarly journals Impact of saline solution on growth and photosystem II during in vitro cultivation of Bromelia antiacantha (Bromeliaceae)

Rodriguésia ◽  
2021 ◽  
Vol 72 ◽  
Author(s):  
Rosiane Cipriano ◽  
João Paulo Rodrigues Martins ◽  
Luiz Carlos de Almeida Rodrigues ◽  
Antelmo Ralph Falqueto ◽  
Andreia Barcelos Passos Lima Gontijo
Keyword(s):  
Photosystem Ii ◽  
Saline Solution ◽  
Growth Traits ◽  
Photosynthetic Apparatus ◽  
Solution Culture ◽  
In Vitro Cultivation ◽  
Ms Medium ◽  
Number Of Leaves ◽  
Positive Effect

Abstract In vitro cultivation is a technique with wide application for micropropagation. However, each species has specific mineral needs for this type of cultivation. The objective was to assess the impacts of the saline solution culture medium on the performance of the photosynthetic apparatus and growth of Bromelia antiacantha during in vitro cultivation, and thus to elucidate the mitigation of the nutritional imbalance that can interfere in the electron transport in the plants. Plants were cultivated in a salt concentration gradient of MS medium (0%, 25%, 50%, 75% or 100%). The growth traits and fluorescence a chlorophyll were analyzed. Intermediate concentrations of MS medium resulted in plants with a larger number of leaves and longer root length. The OJIP curves and results of the JIP test showed that the plants grown without MS salts presented less efficient photosystem II (PSII), as indicated by the performance index [Pi(total)]. In contrast, the intermediate concentrations (MS 25% and 50%) had a positive effect on the performance of the photosynthetic apparatus. The MS 25% medium can be used for in vitro cultivation of B. antiacantha, enabling the development of plants with suitable physiological qualities for planting in the field.

scholarly journals STUDIES WITH HUMAN INFLUENZA VIRUS CULTIVATED IN ARTIFICIAL MEDIUM

1936 ◽  
Vol 63 (6) ◽  
pp. 803-811 ◽  
Author(s):  
T. P. Magill ◽  
Thomas Francis
Keyword(s):  
Influenza Virus ◽  
Neutralizing Antibodies ◽  
The Other ◽  
In Vitro Cultivation ◽  
Human Influenza ◽  
Artificial Medium ◽  
Human Influenza Virus ◽  
Simplified Procedure ◽  
Culture Virus

The in vitro cultivation of strains of human influenza virus has been successfully conducted through a prolonged series of successive transfers. The cultivated virus has retained the antigenic and immunological properties which characterized the animal passage virus from which it was derived. The culture virus is still virulent for mice and ferrets; it is capable of inducing an active state of immunity in animals vaccinated subcutaneously or intraperitoneally; it elicits specific neutralizing antibodies in the serum of infected or vaccinated animals. The virus has been successfully cultivated to date only in the presence of oxygen; when conditions of reduced oxygenation are imposed by the use of vaseline seal, with or without the addition of cystein, multiplication of the virus is not supported. On the other hand, it has been possible to cultivate the virus in the medium of Li and Rivers in ordinary test tubes. This affords a greatly simplified procedure, since the interval between transfers may be prolonged. The results of neutralization tests with various sera and the culture virus are presented and discussed.

scholarly journals STUDIES ON THE COMMON COLD

1936 ◽  
Vol 63 (4) ◽  
pp. 559-579 ◽  
Author(s):  
A. R. Dochez ◽  
K. C. Mills ◽  
Yale Kneeland
Keyword(s):  
Chick Embryo ◽  
Common Cold ◽  
Human Beings ◽  
Anaerobic Conditions ◽  
Gum Acacia ◽  
Human Volunteers ◽  
Destructive Action ◽  
Embryo Tissue ◽  
The Common ◽  
Culture Virus

1. Studies of the cultivation of the virus of common cold in tissue medium, and the capacity of the culture virus to induce infection in human volunteers are reported. 2. Detailed descriptions are given of the methods employed to isolate the virus, preserve and cultivate it, and to test its activity in human volunteers. 3. The virus of common cold can easily be isolated from properly selected patients and cultivated in tissue medium. 4. When kept in the original nasopharyngeal washings, the virus will survive at ice box temperature under anaerobic conditions for at least 13 days. 5. If the nasopharyngeal washings are frozen and dried in vacuo, the virus retains its activity for at least 4 months. 6. The virus of common cold has been proven to multiply in medium containing chick embryo tissue. Such cultures retain their capacity to produce typical infections in human beings for many transfers involving a period of several months. Attempts to cultivate the virus have been successful in seven out of eight instances. 7. Prolonged cultivation of the virus in tissue medium eventually leads to a loss of activity. 8. Strains of virus under cultivation maintain their potency best when transfers are made at 2 and 3 day intervals. 9. After removal from the incubator a culture of virus rapidly becomes inactive whether it be kept under seal in the ice box or frozen and dried in vacuo. 10. The destructive action of the medium can be prevented if the culture is mixed with gum acacia before freezing and drying in vacuo.

scholarly journals THE USE OF YELLOW FEVER VIRUS MODIFIED BY IN VITRO CULTIVATION FOR HUMAN IMMUNIZATION

1937 ◽  
Vol 65 (6) ◽  
pp. 787-800 ◽  
Author(s):  
Max Theiler ◽  
Hugh H. Smith
Keyword(s):  
Tissue Culture ◽  
Yellow Fever ◽  
Antibody Titer ◽  
Yellow Fever Virus ◽  
Fever Virus ◽  
In Vitro Cultivation ◽  
Cultivation In Vitro ◽  
Subcutaneous Inoculation ◽  
Culture Virus

The response of rhesus monkeys to a subcutaneous inoculation with varying amounts of virus modified by prolonged cultivation in vitro has been studied. The tissue components of the medium consisted of chick embryo tissue containing minimal amounts of nervous tissue. The immunity produced in monkeys, as measured by the antibody titer developed, has no relation to the amount of virus inoculated. Monkeys inoculated subcutaneously with the tissue culture virus are rendered immune to a subsequent injection of a highly virulent yellow fever virus. This resistance is already present 7 days after vaccination. The subcutaneous inoculation of the culture virus into immune persons leads to a substantial increase of the serum antibody titer. The results of vaccinating eight normal persons with culture virus are presented. The reactions were minimal. The highest temperature recorded following vaccination was 37.4°C. The sera taken from the eight vaccinated persons 2 to 4 weeks after inoculation with the tissue culture virus showed the presence of yellow fever antibodies.

Sem Studies of Co-Cr-Mo Surgical Implant Alloy Corrosion Behavior

1982 ◽  
Vol 40 ◽  
pp. 520-521
Author(s):  
Ann Chidester Van Orden ◽  
John L. Chidester ◽  
Anna C. Fraker ◽  
Pei Sung
Keyword(s):  
Electron Microscopy ◽  
Corrosion Behavior ◽  
Anodic Polarization ◽  
Saline Solution ◽  
Saturated Calomel Electrode ◽  
Physiological Saline ◽  
X Ray ◽  
Physiological Saline Solution ◽  
Scanning Electron

The influence of small variations in the composition on the corrosion behavior of Co-Cr-Mo alloys has been studied using scanning electron microscopy (SEM), energy dispersive x-ray analysis (EDX), and electrochemical measurements. SEM and EDX data were correlated with data from in vitro corrosion measurements involving repassivation and also potentiostatic anodic polarization measurements. Specimens studied included the four alloys shown in Table 1. Corrosion tests were conducted in Hanks' physiological saline solution which has a pH of 7.4 and was held at a temperature of 37°C. Specimens were mechanically polished to a surface finish with 0.05 µm A1203, then exposed to the solution and anodically polarized at a rate of 0.006 v/min. All voltages were measured vs. the saturated calomel electrode (s.c.e.).. Specimens had breakdown potentials near 0.47V vs. s.c.e.

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