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<strong>Management</strong> <strong>of</strong> <strong>Snakebite</strong> <strong>and</strong> <strong>Research</strong><br />

86<br />

Development <strong>of</strong> Russell’s Viper Toxoid<br />

INTRODUCTION<br />

Khin Maung Maung <strong>and</strong> Win Aung<br />

Biochemistry <strong>Research</strong> Division<br />

Department <strong>of</strong> Medical <strong>Research</strong> (Lower Myanmar)<br />

Abstract<br />

Russell’s viper bite is a serious medical problem in Myanmar. Thus active immunization<br />

<strong>of</strong> persons at risk is <strong>of</strong> utmost importance protective measure. Detoxified venom can be<br />

used as effective toxoid for active immunization. Russell’s viper venom (RVV) toxoid was<br />

first prepared with 0.5% formalin. In 1986 formalinized toxoid prepared with Sephadex<br />

G50 (fine) fractionated RVV were tested on monkeys <strong>and</strong> human volunteers <strong>and</strong> found to<br />

be safe <strong>and</strong> immunogenic. In 1980 RVV toxoid was developed by slow <strong>and</strong> step-wise<br />

formalinization method. The appearance <strong>of</strong> toxicity in formalinized RVV toxoid stored for<br />

one year at different temperature was found in 1994. In 1996 stability <strong>of</strong> Sephadex G75<br />

fractionate RVV was tested at room temperature <strong>and</strong> found to be stable upto six months.<br />

Immunization schedules <strong>and</strong> age <strong>of</strong> the toxoid on immunized animals were also studied<br />

in 1996. In 1997, it was found that RVV toxoid with 35% sodium bisulfite were stable<br />

upto one year at 37°C. RVV toxoid lyophilized <strong>and</strong> stored at room temperature were<br />

found to be less toxic <strong>and</strong> more immunogenic upto one year. Mice immunized with<br />

toxoid prepared by pooling five major enzymes <strong>of</strong> RVV could not withst<strong>and</strong> a lethal dose<br />

<strong>of</strong> RVV.<br />

Russell’s viper (Daboia russelii siamensis) bite has been a serious medical problem in<br />

Myanmar for many decades. Post-bite administration <strong>of</strong> antivenom, a product <strong>of</strong> Myanmar<br />

Pharmaceutical Factory (MPF), is the only effective <strong>and</strong> widely used treatment. However,<br />

the mortality rate remains considerably high. On many occasions, antivenom treatment is<br />

late <strong>and</strong> irreversible damage <strong>of</strong> vital organs has already occurred. Also sometimes, the<br />

development <strong>of</strong> lesion is so rapid that the antivenom alone cannot neutralize the lethal<br />

effect where large amounts <strong>of</strong> venom are already introduced into the body. Therefore,<br />

development <strong>of</strong> a suitable <strong>and</strong> effective measure i.e. active immunization <strong>of</strong> people<br />

susceptible to snakebites is <strong>of</strong> utmost importance as a protective measure. If the victims<br />

are immune to the venom, even to a small degree, the onset <strong>of</strong> damage is delayed <strong>and</strong><br />

they can be treated more successfully (WHO, 1981). Therefore, many attempts have been<br />

made by various scientists to develop <strong>of</strong> RVV toxoid for nearly three decades in Myanmar.

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