Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method and apparatus for location and temperature specific drug action such as thrombolysis

a technology of thrombolysis and temperature, applied in the field of modification and control of optimal temperatures for enzymes, can solve the problems of low cardiac output, severe derangement of the cardiovascular system, and risky systematic vascular effects of use of total body hypothermia

Inactive Publication Date: 2001-08-02
INNERCOOL THERAPIES INC
View PDF0 Cites 79 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the use of total body hypothermia risks certain deleterious systematic vascular effects.
For example, total body hypothermia may cause severe derangement of the cardiovascular system, including low cardiac output, elevated systematic resistance, and ventricular fibrillation.
Other side effects include renal failure, disseminated intravascular coagulation, and electrolyte disturbances.
In addition to the undesirable side effects, total body hypothermia is difficult to administer.
However, use of the Dato device implicates the negative effects of total body hypothermia described above.
However, such methods rely on conductive heat transfer through the skull and into the brain.
One drawback of using conductive heat transfer is that the process of reducing the temperature of the brain is prolonged.
Also, it is difficult to precisely control the temperature of the brain when using conduction due to the temperature gradient that must be established externally in order to sufficiently lower the internal temperature.
In addition, when using conduction to cool the brain, the face of the patient is also subjected to severe hypothermia, increasing discomfort and the likelihood of negative side effects.
It is known that profound cooling of the face can cause similar cardiovascular side effects as total body cooling.
From a practical standpoint, such devices are cumbersome and may make continued treatment of the patient difficult or impossible.
However, external circulation of blood is not a practical approach for treating humans because the risk of infection, need for anticoagulation, and risk of bleeding is too great.
Further, this method requires cannulation of two vessels making it more cumbersome to perform particularly in emergency settings.
Even more, percutaneous cannulation of the carotid artery is difficult and potentially fatal due to the associated arterial wall trauma.
Finally, this method would be ineffective to cool other organs, such as the kidneys, because the feeding arteries cannot be directly cannulated percutaneously.
Perfusion of a cold solution has a number of drawbacks, including a limited time of administration due to excessive volume accumulation, cost, and inconvenience of maintaining the perfusate and lack of effectiveness due to the temperature dilution from the blood.
Temperature dilution by the blood is a particular problem in high blood flow organs such as the brain.
Drug administration is occasionally problematic as some sensitive patients encounter adverse reactions to drugs.
Moreover, there is a risk of hemorrhage when these drugs are given intravenously.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method and apparatus for location and temperature specific drug action such as thrombolysis
  • Method and apparatus for location and temperature specific drug action such as thrombolysis
  • Method and apparatus for location and temperature specific drug action such as thrombolysis

Examples

Experimental program
Comparison scheme
Effect test

example two

[0114] (Non-drug)

[0115] In another non-drug study of the effect of temperature on fibrinolysis, clot lysis in dogs was investigated while varying clot temperatures in a range of 20.degree. C. to 36.degree. C. The dog's temperature was lowered from a normal temperature to a low temperature. A gradual rewarming period followed the low temperature period.

[0116] Enhanced clot lysis was observed at lower temperatures as compared to higher temperatures. In particular, the maximum fibrinolytic activity occurred in the early rewarming period, i.e., from 20.degree. C. to about 25.degree. C. It is believed that this study can be extended to humans, and that fibrinolytic activity can be enhanced at lower temperatures, especially during periods of rewarming.

[0117] An advantage of all of these embodiments of the method is that clot lysis can be achieved in a simple manner and without the need for drugs. An additional advantage results from the reduced temperature of the blood which helps to prot...

example three

[0124] (SK)

[0125] Researchers have investigated the effect of temperature on the fibrinolytic activity of an SK mixture. In one such effort, clots were treated with a mixture of plasminogen (2 mg) and SK (100 IU) in a total volume of 15 ml PBS. The temperature of the clots was raised from 24.degree. C. to 37.degree. C. These researchers found that heating enhanced the fibrinolytic activity. In other words, heating from a hypothermic temperature to normal body temperature increased clot lysing for clots treated with SK.

[0126] It is believed that such general trends may be extended to patients without lack of accuracy. Patients may be provided with a drug such as streptokinase and may undergo hypothermia using, e.g., one of the devices or methods described above. In particular, a cooling catheter may be placed in an artery supplying blood to a thrombosed vessel. The catheter may include a separate lumen through which the SK mixture may be delivered. A coolant or working fluid may be s...

example four

(tPA)

[0127] Researchers have also investigated the effect of temperature on the fibrinolytic activity of tPA. Clots were treated with 2.5 .mu.g / ml tPA and incubated at various temperatures (e.g., 37.degree. C., 25.degree. C., 10.degree. C., 0.degree. C., and -8.degree. C.). Plasminogen activation was relatively high at low temperatures (e.g., 0.degree. C. or -8.degree. C.) and was much less at higher temperatures. In other words, these researchers found that, for tPA, cooling to a hypothermic temperature from normal body temperature increased fibrinolytic activity.

[0128] As above, it is believed that such trends may be extended to patients without lack of accuracy. In this case, patients may be provided with tPA and may undergo hypothermia using an above device placed in an artery supplying blood to a thrombosed vessel. The catheter may include a separate lumen through which tPA may be delivered. A coolant or working fluid may be supplied to the cooling catheter, causing the cathete...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

A method is provided of localizing a drug action where the drug is present throughout a vascular system. The localization occurs to within a volume of blood in a blood vessel, the vascular system having an initial temperature substantially within a first temperature range. A temperature-specific enzyme is delivered throughout a vascular system including a volume of blood in a blood vessel, the temperature-specific enzyme having a working temperature within a prespecified temperature range that does not substantially overlap the first temperature range. A heat transfer element is delivered to a blood vessel in fluid communication with the volume of blood. The temperature of the heat transfer element is adjusted such that the volume of blood in the blood vessel is heated or cooled to the prespecified temperature range. In this way, the action of the temperature-specific enzyme is substantially limited to the volume of blood heated or cooled. In an alternative embodiment, the temperature-specific enzyme is localized to the volume of blood in the blood vessel, and the heat transfer element is disposed in fluid communication with the volume of blood in the blood vessel. The enzyme localization may occur by way of direct injection or by way of injection through a lumen of a catheter. The injection lumen of the catheter may be disposed at least partially adjacent or in combination with the heat transfer element and its associated inlet and outlet lumens.

Description

[0001] This application is a divisional of U.S. patent application Ser. No. 09 / 232,177, filed Jan. 15, 1999, and entitled "Method and Apparatus for Location and Temperature Specific Drug Action Such as Thrombolysis", which is a continuation-in-part patent application of co-pending U.S. patent application Ser. No. 09 / 215,039, filed Dec. 16, 1998, and entitled "Method for Low Temperature Thrombolysis and Low Temperature Thrombolytic Agent with Selective Organ Temperature Control"; U.S. patent application Ser. No. 09 / 215,040, filed Dec. 16, 1998, and entitled "Method and Device for Applications of Selective Organ Cooling"; U.S. patent application Ser. No. 09 / 103,342, filed Jun. 23, 1998, and entitled "Selective Organ Cooling Catheter and Method of Using the Same"; U.S. patent application Ser. No. 09 / 047,012, filed Mar. 24, 1998, and entitled "Selective Organ Hypothermia Method and Apparatus"; and U.S. patent application Ser. No. 09 / 052,545, filed Mar. 31, 1998, and entitled "Circulatin...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): A61F7/00A61F7/12
CPCA61B2018/0212A61B2018/0262A61B2018/0281A61F7/12A61F2007/0056A61F2007/126
Inventor DOBAK, JOHN D. IIILASHERAS, JUAN C.
Owner INNERCOOL THERAPIES INC
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products