Drug – bio-affecting and body treating compositions – Effervescent or pressurized fluid containing – Organic pressurized fluid
Reexamination Certificate
2000-08-10
2004-04-13
Page, Thurman K. (Department: 1616)
Drug, bio-affecting and body treating compositions
Effervescent or pressurized fluid containing
Organic pressurized fluid
C424S400000, C424S489000, C424S450000, C514S951000
Reexamination Certificate
active
06719960
ABSTRACT:
This invention relates to medicaments for and methods of reducing the probability of surgical adhesions.
Following surgery, membranes which have been severed may ‘cross-heal’. For example the abdominal wall can heal with the peritoneum and adhere to it. This is known as an adhesion. A very serious complication of adhesions inside the peritoneum is intestinal obstruction. Unless corrected surgically this can rapidly be fatal. It has been estimated that in the US in 1988 the cost of correcting lower abdominal pelvic adhesions was of the order of US$ 1180 million (AH De Cherney and GS diZeregram Surgical Clinics of North America 77(3), 671). Attempts have been made to reduce adhesions by providing physical barriers such as sheets of hyaluronic acid and carboxymethylcellulose. While providing an initial barrier the sheets degrade.
It has now been unexpectedly found that natural occurring surface active phospholipids and enantiomers thereof can substantially reduce the likelihood of adhesions forming.
According to the invention there is provided a method of reducing the probability of surgical adhesion comprising administering SAPL to mesothical membranes during surgery.
According to the invention there is provided the use of a SAPL in the manufacture of a medicament for use in reducing the probability of surgical adhesions following surgery.
Embodiments of the invention will be described by way of non-limiting example by reference to the Figure which shows the length of adhesion formed under various conditions.
A physical or chemical binding of the surfictant to the membrane is highly desirable. Examples of suitable phospholipids include diacyl phosphatidyl cholines (DAPC's) such as dipalmitoyl phosphatidyl choline (DPPC), dioleyl phosphatidyl choline (DOPC) and distearyl phosphatidyl choline (DSPC). It is also preferred to include a spreading agent in the composition to assist the DPPC or analogous compound rapidly to form a thin film over the surface of the membrane. A number of agents are capable of acting in this way including other phospholipids, such as phosphatidylglycerols (PG); phosphatidylethanolamines (PE); phosphatidylserines (PS) and phosphatidylinositols (PI). Another useful spreading agent is cholesteryl palmitate (CP). We prefer to use dipalmitoyl phosphatidyl choline (DPPC) and unsaturated phosphatidyl glycerol (PG) either alone or in combination. A mixture comprising DPPC 70 wt % and PG 30 wt % can be used. This material is commercially available as ALEC™ from Britaia Pharmaceutical Limited. ALEC is known for use in treating respiratory distress syndrome see for example British Medical Journal 294 (1984) 991-996.
A widely accepted theory on the mechanism of action of ALEC in the lungs of neonates is that it functions principally by lowering surface tension Since there is no air-water interface in the normal peritoneal cavity one would not expect ALEC and other SAPL's to be effective in preventing the formation of or reduction the probability of forming adhesions. It has however been experimentally found that SAPL's do, in fact reduce the frequency of adhesion formation as will become apparent from the experimental data set forth below.
40 rabbits were taken. A surgical opening was made in the peritoneum Opposing peritoneal surfaces were subjected to a sterilised 50 mm abrasion. In 10 cases the opening was simply closed. In a further 10 cases the abrasion was perfused with dialysate prior to closure. In a still further 10 cases the abrasion was perfused with a suspension of ALEC in dialysate and the opening closed. In a final 10 cases powdered ALEC was blown into the abrasion prior to closure. Following healing the peritoneum was reopened and the presence of adhesions noted. Where adhesions were noted their length was measured. The results are shown in Table 1.
TABLE 1
Control
Dialysate
ALEC & Dialysate
ALEC
Number of adhesion
1
5
4
5
free cases
Total length of
320
197
151
91
adhesion (mm)
Reduction in
—
38%
53%
72%
adhesion length
relative to control
Mean Adhesive
32
19.7
15.1
9.1
Length (mm)
Standard Deviation
5
10.5
9
5
One can say therefore with a high degree of confidence (even with a very limited number of samples) that ALEC powder markedly reduces both the likelihood of adhesion formation and the length of the adhesions which do form. There is also evidence that a suspension of ALEC is more effective than either no treatment or treatment with dialysate.
Preferably the SAPL is used in the form of a dry powder aerial dispersion.
Phosphatidyl glycerol (PG) is believed to be capable of binding to the surface of the animal tissue and is, therefore, a preferred component of the SAPL. Dipalmitoyl phosphatidyl choline (DPPC) may function also in this way and is also a preferred compound of the SAPL. PG has a further important function in medicaments employed in the present invention which is its ability to cause the DPPC to form a dry powder. The particle size of such powders is not critical and the controlling factor is that the size is preferably such that medicament can be readily instilled into the surgical site. Generally, the particle size is within the range of 0.5 to 100 &mgr;M. Particles which are more readily conveyed in a gas stream have a particle size of from 0.5 to 20 &mgr;m, preferably 0.5 to 10 &mgr;m and more preferably 0.5 to 2 &mgr;m. Finely-divided dry powders of this kind are believed to be absorbed very rapidly onto the surfaces of mesothical membranes, i.e. bound to the epithelium. Preferably, the SAPL compositions employed in the present invention are blends of dipalmitoyl phosphatidyl choline (DPPC) and PG, although as indicated above, other phospholipids may be employed.
The medicament should generally be essentially free from animal protein in order to avoid the danger of patient sensitivity to animal proteins. Also, animal proteins may become adhesive and, for this reason, should preferably be excluded from the compositions.
DPPC is commercially available from Sigma Chemical Co. Ltd. or can be prepared synthetically by the use of acyl chlorides using the method of Baer & Bachrea—Can. J. Of Biochem. Physiol 1959; 37, page 953 and is available commercially from Sigma (London) Ltd. The PG may be prepared from egg phosphatidyl choline by the methods of Comfurions et al and Dawson, Biochem. Biophys Acta 1977; 488; pages 36-42 and Biochem J. 1947; 192; pages 205-210.
The medicaments employed in the present invention are generally finely-divided dry powders having a particle size distribution which is small enough to be introduced into the surgical site in a gas stream from a dispersion device. The material available commercially as ‘Alec’ has a particle size distribution such that a major proportion is between 0.5 and 2 &mgr;m with a median particle diameter of about 1.2 &mgr;m. However, as mentioned above, larger particle size powders can be satisfactorily used in accordance with the invention. The medicament of the present invention may be introduced into the surgical site through a cannula, e.g. connected to a syringe.
However, we prefer to employ a dispersion device which utilises a propellant. These may employ a propellant such as a halocarbon to form a gas stream and may include a tapered discharge nozzle, baffle or venturi to accelerate particles through a discharge nozzle. Suitable halocarbons include hydrofluorocarbons, hydro-fluorochlorocarbons and fluorochlorocarbons having a low boiling point, such as those marketed by DuPont under the trade marks “Freon” and “SUVA”. Pharmaceutically acceptable hydrofluoroalkanes are available as HFA-134a and 227.
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Snoj et al., “Effect of . . . in the rat”. Br. J. Surg. 79:427-429, 1992.
Ar Rajab et al., “Phosphatidylcholine . . . in the rat”, J. Surg. Res.
Hills Brian Andrew
Woodcock Derek Alan
Britannia Pharmaceuticals Ltd.
Gollamudi Sharmila S
GrayCary LLP
Nakamura Dean H.
Page Thurman K.
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