Microbial air sampler integrating media plate and sample collection device

Patent metadata

Field	Value
Publication number	US-10345200-B2
Application number	US-201414338615-A
Country	US
Kind code	B2
Filing date	Jul 23, 2014
Priority date	Jul 23, 2013
Publication date	Jul 9, 2019
Grant date	Jul 9, 2019

Abstract

The invention generally provides devices and methods for sampling, detecting and/or characterizing particles, for example, via collection, growth and analysis of viable biological particles such as microorganisms. Devices and methods of the invention include particle samplers and impactors for collecting and/or analyzing biological particles in manufacturing environments requiring low levels of particles, such as cleanroom environments for electronics manufacturing and aseptic environments for manufacturing pharmaceutical and biological products, such as sterile medicinal products. Devices and methods of the invention incorporate an integrated sampler and impact surface, such as the receiving surface of a growth media, in a manner to minimize, or entirely eliminate, risks associated with user handling, such as the occurrence of false positive determinations due to contamination of the impact surface during particle sampling, growth or analysis processes.

First claim

We claim:

1. A method for sampling biological particles from a fluid flow, said method comprising the steps of:
sterilizing an impactor, said impactor comprising:
a sampling head comprising one or more intake apertures for sampling said fluid flow containing said biological particles; and
an impactor base operationally connected to receive at least a portion of said fluid flow from said sampling head; said impactor base comprising an impact surface positioned to receive at least a portion of said biological particles in said fluid flow and an outlet for exhausting said fluid flow, and said impactor base comprising a growth medium positioned to receive said particles in said fluid flow, wherein said impact surface is a receiving surface of said growth medium;
a transparent selectively removable cover provided on said sampling head and covering said intake apertures;
wherein said sampling head and said impactor base are integrated components that engage to enclose said impact surface, wherein at least a portion of said impactor base and said sampling head each comprise a polymer material and are optically transparent; and
wherein said impactor is sterilized by irradiating the impactor in a fully assembled configuration, wherein said growth medium is present within the impactor base and is sterilized by the sterilizing step, and said selectively removable cover on said sampling head maintains a sterile environment for said growth medium prior to sampling said fluid flow containing particles;

removing said selectively removable cover on said sampling head;
sampling said fluid flow with said impactor, wherein said outlet is laterally adjacent to said impact surface and wherein a direction of the fluid flow changes by more than 40 degrees after passage through said one or more intake apertures;
growing at least a portion of said biological particles received by said growth medium until said biological particles are visible by eye or detectable using an optical detector or imaging device;
counting said grown particles visually or using an optical detector or imaging device; and
characterizing at least a portion of said grown particles by visualization, optical detection or imaging and determining viability and identity of microorganisms in said grown particles;
wherein said sterilizing step, growing step, counting step, characterizing step, and determining step are carried out without disengaging said sampling head and said impactor base.

2. The method of claim 1 wherein said characterizing step further comprises determining the size of the biological particles received by said impact surface.

3. The method of claim 1 wherein said characterizing step is performed by said imaging device.

4. The method of claim 1 , wherein the impactor base has a height of 22 mm to 24 mm and an area of 10,730 mm 2 to 10,760 mm 2 .

5. The method of claim 4 , wherein said growth medium is provided in a petri dish comprising an integrated component of said impactor base.

6. The method of claim 5 , wherein said petri dish is cast in a single piece with the impactor base.

7. The method of claim 4 , wherein said growth medium comprises an agar plate.

8. The method of claim 4 , wherein said sampling head and said impactor base engage to entirely contain said impact surface.

9. The method of claim 1 , wherein said method does not include a user physically contacting said growth medium after it has been contacted with said particles.

10. The method of claim 1 , further comprising the step of repositioning said selectively removable cover on said sampling head for covering said intake apertures, thereby sealing said growth medium after said sampling step.

11. The method of claim 1 , comprising sampling said fluid containing said particles using said impactor for a single use only.

12. The method of claim 1 , comprising monitoring biological particles in cleanroom or aseptic environments.

13. The method of claim 1 , comprising monitoring biological particles in air or one or more process gases.

14. The method of claim 1 , further comprising repeating the steps of the method using a new sampler.

15. The method of claim 1 , wherein said sampling head and said impactor base engage via a substantially airtight seal.

16. The method of claim 1 , wherein said impactor base has a plurality of grooves provided on an outer surface to allow for effective handling of the impactor by a user.

17. The method of claim 1 , wherein said impactor base has one or more recessed features to allow for effective stacking of a plurality of said impactors.

18. The method of claim 1 , wherein said one or more intake apertures comprise a plurality of slits arranged in a circular pattern.

19. The method of claim 1 , wherein said counting step is performed using an optical particle counter.

20. A method for sampling biological particles from a fluid flow, said method comprising the steps of:
providing an impactor comprising:
a sampling head comprising intake apertures for sampling a fluid flow containing particles, wherein said intake apertures comprise twenty slits arranged in a circular pattern, each slit having a width of 0.1 mm; and
an impactor base operationally connected to receive at least a portion of said fluid flow from said sampling head; said impactor base comprising a support having an impact surface for receiving at least a portion of said particles in said fluid flow and an outlet for exhausting said fluid flow, wherein said impactor base has a height of 22 mm to 24 mm and an area of 10,730 mm 2 to 10,760 mm 2 , and further comprises a growth medium positioned to receive said particles in said fluid flow and said support for accommodating the growth medium, wherein said impact surface is a receiving surface of said growth medium and said support has a height of 17 mm-19 mm and a volume of 20 ml-40 ml;
a transparent selectively removable cover provided on said sampling head and covering said intake apertures;
wherein said sampling head and said impactor base are integrated components that engage to enclose said impact surface, wherein at least a portion of said impactor base and said sampling head each comprise a polymer material and are optically transparent;

sterilizing said impactor in a fully assembled configuration by irradiating the fully assembled impactor using beta radiation wherein said impact surface remains enclosed by said sampling head and impactor base during sterilization, and wherein said growth medium is present within the impactor base and is sterilized by the sterilizing step, and said selectively removable cover on said sampling head maintains a sterile environment for said growth medium prior to sampling said fluid flow containing particles;
removing said selectively removable cover on said sampling head;
sampling said fluid flow with said impactor, wherein particles in said fluid are received by said impact surface, wherein said outlet is laterally adjacent to said impact surface and a direction of the fluid flow changes by more than 40 degrees after passage through said intake apertures; and
growing at least a portion of said biological particles received by said growth medium until said biological particles are visible by eye or detectable using an optical detector or imaging device;
counting said grown particles visually or using an optical detector or imaging device; and
characterizing at least a portion of said grown particles by visualization, optical detection or imaging and determining viability and identity of mic

Assignees

• Particle Measuring Syst
• Particle Measuring Systems S R L

Inventors

• Scialo Giovanni
• Adkins Ronald W
• Recchia Davide

Classifications

• C12N5/0665

  Blood-borne mesenchymal stem cells, e.g. from umbilical cord blood · CPC title

• A61K35/51

  Umbilical cord; Umbilical cord blood; Umbilical stem cells · CPC title

• G01N15/0612

  Optical scan of the deposits (G01N15/0625 takes precedence) · CPC title

• G01N15/0227

  using imaging; using holography · CPC title

• G01N21/9515

  Objects of complex shape, e.g. examined with use of a surface follower device (measuring contours and curvatures G01B11/24) · CPC title