Composition and method for medical imaging or body cavities

Abstract

The present invention relates to an image enhancing composition for the enhancement of contrast in a body cavity, wherein the viscosity of the composition is between 2000 and 4000 mPa.Math.sec. It also relates to a method for enhancing contrast of an image of a body cavity, which method comprises introducing one single small amounts of an image enhancing composition into the body cavity. In another aspect, the present invention provides a high contrast image of a body cavity obtained by the method of the invention, in particular a 3-dimensional high contrast image.

Claims

1. An echo-lucent image enhancing composition for the enhancement of contrast in a body cavity, wherein the composition comprises a cellulose derivative has a pH between 5.5 to 7.5 and a viscosity between 2000 to 4000 mPa.Math.sec. when measured at room temperature wherein the composition is free of particulate matter that interfere with clear image formation.

2. The echo-lucent image enhancing composition according to claim 1, wherein the viscosity of the composition is between 2700 and 3000 mPa.Math.sec, when measured at room temperature.

3. The echo-lucent image enhancing composition according to claim 1, wherein the composition is free of pyrrolidones, alcohols, disinfectants and anaesthetics.

4. The echo-lucent image enhancing composition according to claim 1, wherein the cellulose derivative is hydroxyethylcellulose or methylcellulose.

5. The echo-lucent image enhancing composition according to claim 1, wherein the composition provides enhancement of contrast in a uterine cavity.

6. The echo-lucent image enhancing composition according to claim 1, wherein the composition provides for three dimensional imaging.

7. A method for enhancing contrast of an image of a body cavity, comprising the step of introducing an echo-lucent image enhancing composition according to claim 1 into the body cavity.

8. The method according to claim 7, wherein the imaging is 3-dimensional imaging.

9. The method according to claim 7, wherein the imaging is an imaging procedure of the uterine cavity.

10. The method according to claim 9, wherein the imaging procedure comprises ultra-sound imaging.

11. A method for enhancing contrast of an image of a body cavity, comprising the step of introducing once 1-10 ml of an echo-lucent image enhancing composition according to claim 1 into the body cavity.

12. A high contrast image of a body cavity, wherein the high contrast image is a 3-dimensional image obtained by the method of claim 11.

13. The method according to claim 9, wherein the imaging procedure is sonohysterography.

14. A method for enhancing contrast of an image of a body cavity, comprising the step of introducing once 3-5 ml of an echo-lucent image enhancing composition according to claim 1 into the body cavity.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIGS. 1a-1d

(2) Illustrate a three dimensional picture of a uterus, wherein the picture was made using a gel composition according to the invention and a clear and sharp image without artifacts is obtained.

(3) FIG. 2

(4) Illustrates a two dimensional picture of a uterus, wherein the picture is made using conventional medium and three dimensional pictures are not possible with conventional medium because it would contain many artifacts due to a high flow of the medium.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

(5) The present invention relates to an image enhancing composition for the enhancement of contrast in a body cavity, wherein the viscosity of the composition is between 2000 and 4000 mPa.Math.sec.

(6) One of the advantages of the image enhancing compositions of the invention is that they overcome the inconveniences and discomfort caused by saline infusions. With these state of the art saline infusions fluid leakage frequently occurs if a catheter is used, or pain is experienced due to pressure of a balloon catheter.

(7) Another advantage is that only small aliquots of the compositions according to the invention are needed to achieve an optimal distension of a body cavity.

(8) Due to a much smaller leakage velocity in comparison to saline, examination of the cavity is possible for several minutes, even after removal of the installation device. Compositions of the invention have a viscosity of between 2000 and 4000 mPa.Math.sec. as determined by standard viscosity determination methods, measured at room temperature and under atmospheric pressure. In one embodiment, the viscosity of the composition of the invention is between 2500 and 3500, preferably between 2700 and 3000 mPa.Math.sec. More preferably, the viscosity of a composition of the invention is between 2800 and 2900 mPa.Math.sec. when measured at room temperature. At body temperature the viscosity of a composition of the invention will be lower. Preferably, the viscosity will be between 2300 and 2500 mPa.Math.sec. most preferably it will be between 2400 and 2500 mPa.Math.sec. when measured at body temperature.

(9) Image enhancing compositions of the invention may be used for all types of medical imaging, including X ray imaging, echography, magnetic resonance imaging, CT scanning and ultrasound imaging. Preferably, they are used for ultrasound imaging. More preferably, it is used for 3-dimensional ultrasound imaging.

(10) As used herein, “image enhancement” refers to increasing the contrast of an image. The contrast enhancement may be either negative (black) or positive (white).

(11) Typically, enhancement also involves distension of the body cavity of which an image is made. The compositions of the invention may be used for the imaging of any body cavity, including each part of the gastro-intestinal tract, such as the stomach, the colon. the duodenum; the bladder, the vagina. In a preferred embodiment, the body cavity is the uterine cavity.

(12) Compositions of the invention should consist of substances which are safe for use in the human or animal body. They should be echo-lucent and the should therefore not contain particulate material, such as starch. Suitably, compositions of the invention are clear and do not contain particles, bubbles or protein, which will disturb the signal.

(13) In one embodiment, the composition of the invention comprises a cellulose derivative, such as hydroxyethylcellulose or methylcellulose, in a buffer. Preferably, the composition comprises hydroxyethylcellulose. It is important that the composition contains so much of the cellulose derivative to achieve a viscosity of between 2000 and 4000 mPa.Math.sec. as determined by standard viscosity determination methods, measured at room temperature and under atmospheric pressure, preferably between 2500 and 3500, or between 2700 and 3000 mPa.Math.sec. More preferably, enough to achieve a viscosity of between 2800 and 2900 mPa.Math.sec. when measured at room temperature. At body temperature, a viscosity of between 2300 and 2500 mPa.Math.sec., most preferably of between 2400 and 2500 mPa.Math.sec. should be achieved.

(14) The skilled person will understand that adjuvants, such as disinfectants or a local anaesthetic, may be added, for instance glycerine, lidocaine and chlorohexidine. In addition contrast enhancers may be added, such as iodine for X-ray imaging. However, in a preferred embodiment of the invention the composition consists substantially of a cellulose derivative, such as hydroxyethylcellulose or methylcellulose in a buffer, and no other adjuvants such as alcohol, polyvidone, lidacoine, or related compounds.

(15) The pH value of the composition is between about 5.5 and about 7.5. Preferably, between about pH 6.0 and about 7.0, more preferably between about pH 6.3 and about 6.8.

(16) In another aspect, the compositions of the invention may be used to manufacture an image enhancing medium for use in a medical imaging procedure. The composition may advantageously be used in 3-dimensional imaging procedures. In one embodiment, the compositions of the invention are used in 3-dimensional sonohysterography. In another aspect, the invention provides for the use of an image enhancing composition according to the invention for enhancing contrast of an image of a body cavity. The method comprises introducing one single small aliquot of a medium comprising the composition of the invention in the body cavity. The skilled person will understand that the amount which has to be administered or introduced will be dependent on the size of the body cavity which has to be imaged. Typically, about 1-about 10 ml will be enough for most body cavities. In one embodiment, about 3-about 5 ml of an image enhancing composition according to the invention is used for ultrasonic examination of the uterine cavity. Constant infusion of the composition is not necessary, which is a great advantage of the method of the present invention.

(17) A medium comprising a compositions of the invention may be administered or introduced in a body cavity by methods known in the art and depending on the body cavity which is to be examined. For instance, for examination of the uterus, the composition is typically administered via an instillation device, such as a catheter.

(18) In yet another aspect, the invention provides for high contrast images which are obtainable by using the compositions of the invention. Also encompassed in the invention, are high contrast 3-dimensional images. In particular, high contrast 3-dimensional images of the bladder, gastro-intestinal tract and the uterus. In a preferred embodiment, the invention is used for so-called virtual hysteroscopy. Three dimensional imaging requires a very stable and quiet filling of the cavity of interest, with a minimum amount of artefacts. The gel and method of the invention enables this.

EXAMPLE

(19) This example demonstrates how the compositions and method of the invention may effectively and safely be used for sonohysterography.

(20) The composition used for sonohysterography was a sterile, clear viscous gel containing hydroxyethylcellulose, glycerin, lidocaine (2% w/w) and chlorohexidine (0.05% w/w) buffered with acetic acid.

(21) The composition was instilled using a cheap and easy to handle instillation device developed with a back-flow valve and flexible cervical adaptation, preventing leakage of the gel to the vagina. However, state of the art installation devices may be used instead.

(22) The ultrasonic properties of the gel appeared comparable to saline in the first 120 patients. With only about 4 ml already an optimal distension could be achieved (range 2-10 ml). The gel could therefore be instilled from a normal 10 ml syringe fixed to the device and carefully flushed prior to the instillation preventing the introduction of air bubbles. Due to a much slower leakage velocity as compared to saline, ultrasonographic examination of the uterine cavity was possible for a long time even after removal of the instillation device. Only in a few cases a quick collapse of the uterine cavity was seen directly after removal of the device. This also illustrated that there was hardly any leakage of the gel through the Fallopian tubes. Installation of the gel was less painful as compared to the introduction of a balloon catheter. This shows that gel instillation is an alternative for saline infusion and can be used effectively and safe for sonohysterography. Gel instillation sonohysterography offers a more stable filling of the uterine cavity allowing detailed examination without inconveniences.