PharmaSat

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PharmaSat
PharmaSat undergoing preflight testing
Mission typeBiological research
OperatorNASA
COSPAR ID2009-028B Edit this at Wikidata
SATCAT no.35002
WebsitePharmaSat
Mission duration6 months (planned)
3 years, 2 months, 25 days (final)
Spacecraft properties
Bus3U CubeSat
ManufacturerNASA Ames Space Center
Launch mass4.5 kg (9.9 lb)
PowerSolar cells and batteries
Start of mission
Launch date19 May 2009, 23:55 UTC[1][2]
RocketMinotaur I
Launch siteMARS, Pad 0B
ContractorOrbital Sciences
End of mission
Decay date14 August 2012
Orbital parameters
Reference systemGeocentric orbit[3]
RegimeLow Earth orbit
Perigee altitude428 km (266 mi)
Apogee altitude466 km (290 mi)
Inclination40.4°
Period93.52 minutes

PharmaSat was a nanosatellite developed by NASA Ames Research Center which measured the influence of microgravity upon yeast resistance to an antifungal agent. As a follow on to the GeneSat-1 mission, the Ames Small Spacecraft Division conducted the PharmaSat mission in collaboration with industry and local universities.[4]

PharmaSat was the first nanosatellite to implement biological science guided by its Principal Investigator. The mission was designed to aid the development of medicines or techniques to enable long-term crewed space travel and habitation.

The PharmaSat mission builds upon technology demonstrated by GeneSat-1, which used a CubeSat to study microfluidics and optics in the space environment. It was designed to provide life-support, growth, monitoring, and analysis capabilities for microorganisms.

Based, like GeneSat-1, around a three-unit CubeSat platform; PharmaSat was designed to accomplish five functions in an autonomous free-flying platform:[4]

  1. Provide life support and environmental control for growth of the yeast strain in 48 independent microwells;
  2. Dose the growing yeast with antifungal agent at the appropriate point on the growth curve with three distinct, well-defined dosage levels, plus a zero-dose control;
  3. Track the population of the yeast via optical density of each microwell before, during and after antifungal administration;
  4. Determine well-by-well yeast viability at multiple, well-defined times after antifungal administration using a colorimetric reagent, Alamar Blue;
  5. Telemeter the resulting population and viability data to Earth, along with system status data.

Operations

See also

References

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