Process for detecting pathogens

Claim 2

Process for the detection of pathogens, such as bacteria, fungi and viruses, in blood in the presence of an anticoagulant agent which comprises: separating a pathogen in an extracorporeal circulation of the blood, by passing the blood through a sterile adsorbent which is nontoxic and inert to blood and which selectively binds the pathogen while the blood passes the adsorbent; and thereafter detecting the adsorbed pathogen while still culturable.

Claim 3

Process of claim 1 wherein the adsorbent is a polymer which selectively binds the pathogen, the polymer optionally being applied to a porous carrier.

Claim 4

Process of claim 2 wherein the polymer is selected from the group of polyacrylate, polymethacrylate, polyhydroxyethyl methacrylate, an adsorber resin, synthetic crosslinked polystyrene, cellulose acetate, collodion and nylon.

Claim 5

Process of claim 2 wherein the porous carrier in glass, a ceramic material, a metal oxide, silicon dioxide or active charcoal.

Claim 6

Process of claim 1 wherein the adsorbent is active charcoal coated wholly or partly with a polymer selected from the group of polyacrylate, polymethacrylate, polyhydroxyethyl methacrylate, an adsorber resin, synthetic crosslinked polystyrene, cellulose acetate, collodion and nylon.

Claim 7

Process of claim 5 wherein the coating amounts to 0.5 to 10% of the total weight of the adsorbent.

Claim 8

Process of claim 6 wherein the coating amounts to about 2% of the total weight of the adsorbent.

Claim 9

Process of claim 1 wherein the adsorbent is a porous material coated with vapor deposited charcoal.

Claim 10

Process of claim 8 wherein the adsorbent is glass coated with vapor deposited charcoal.

Claim 11

Process of claim 1 wherein the adsorbent is glass coupled with heparin and/or albumin.

Claim 12

Process of claim 1 wherein the pathogen is detected by bacteriological, mycological, virological or electron microscopic methods.

Claim 13

Process of claim 1 wherein the pathogen is detected in the adsorbed state by microbiological, virological or electron microscopic investigation.

Claim 14

Process of claim 12 wherein the detection of the pathogen takes place by introducing the adsorbent enriched with the pathogen into an appropriate nutrient medium and, after incubation, identification takes place by known bacteriological, mycological or electron microscopic techniques.

Claim 15

Process of claim 12 wherein the detection of the pathogen is carried out by culturing the adsorbent enriched with the pathogen in egg cultures, and thereafter identification is carried out by means of known virological techniques.

Claim 16

Process of claim 12 wherein, for the detection of the pathogen, the adsorbent enriched with the pathogen is washed with a buffer, dehydrated with alcohol, treated with a buffered solution of glutaraldehyde and investigated by raster electron microscopy.

Claim 17

Process for detecting the presence of a pathogen selected from the group consisting of bacteria, fungi and viruses, in blood, as a means of early medical diagnosis of sepsis which comprises, extracorporeally circulating blood under investigation in the presence of an anticoagulant through a bed of a sterile particulate material which is nontoxic and inert to blood and effective to selectively bind a pathogen in the blood while the blood passes the adsorbent, permitting said material to bind any pathogen in the blood, recovering the material with any pathogen found or immobilized thereon while the pathogen is still culturable, and analyzing the material to detect any bound or immobilized pathogen.

Claim 18

Process for detecting the presence of a pathogen selected from the group consisting of bacteria, fungi and viruses, in blood, as a means of early medical diagnosis of sepsis which comprises, extracorporeally circulating blood under investigation in the presence of an anticoagulant through a bed of a sterile particulate material which is nontoxic and inert to blood and effective to selectively bind a pathogen in the blood while the blood passes the adsorbent, permitting said material to bind any pathogen in the blood, recovering the material with any pathogen found or immobilized thereon while the pathogen is still culturable, and analyzing the material to detect any bound or immobilized pathogen.

Claim 19

Process of claim 16 wherein said bed has a volume of 5 to 100 cm 3 .

Claim 20

Process of claim 16 wherein said material comprises a vegetable charcoal coated with acrylic hydrogel.

Claim 21

Process of claim 16 wherein said analyzing is carried out bacteriologically, mycologically, virologically or by electron microscope.