Epidural administration of therapeutic compounds with...

Surgery – Means for introducing or removing material from body for... – Treating material introduced into or removed from body...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C604S500000, C424S450000, C424S457000

Reexamination Certificate

active

06428529

ABSTRACT:

THE FIELD OF THE INVENTION
This invention relates to controlled release of therapeutic compounds from drug delivery systems. More particularly, this invention relates to epidural administration of therapeutic compounds with sustained rate of release from a liposome formulation. This invention further relates to method of epidural catheter placement in a living vertebrate.
BACKGROUND
Post-operative pain management is a serious issue for patients and physicians, especially in the recovery room, as the patient is waking up from the anesthesia. Too generous a dose of systemic opioid given in an attempt to control pain can potentially cause life-threatening respiratory depression. On the one hand, either too little or too late a dose of post-operative pain medication can result in the patient waking up in intolerable severe pain. In addition, it has been shown that poorly controlled post-operative pain following abdominal or thoracic surgery inhibits ventilatory movement of the chest wall abdomen, and diaphragm, (P. R. Bromage,
Textbook of Pain,
P. D. Wall, et al. (Eds.): Churchill Livingstone, 1989, pp 744-753) resulting in pulmonary atelectasis.
The existence of opioid receptors in the spinal cord was discovered in the 1970's. Following initial clinical efficacy reports in 1979 (M. Behar et al.,
Lancet
1:527-529, 1979), epidural opioid administration has become very popular for post-operative pain control (T. I. Ionescu et al.,
Act. Anaesth. Belg.
40:65-77, 1989; C. Jayr et al,
Anesthesiology
78:666-676, 1993; S. Lurie, et al.
European Journal of Obstetrics and Gynecology and Reproductive Biology
49:147-153, 1993). Epidural opioids have the advantage of achieving good local analgesia at the spinal level without the loss of locomotor or vasomotor control or decreased level of consciousness.
Injectable opioids are widely used epidurally in post-operative and post-partum settings. Post-operative and postpartum pain usually lasts several days, but injectable opioids have relatively short durations of action (W. G. Brose et al.,
Pain
45:11-15, 1991; R. H. Drost et al.,
Arzneim-Forsch/Drug Res.
38:1632-1634, 1988; G. K. Gourlay et al.,
Pain
31:297-305, 1987). Thus, either continuous infusion or repeated injections are required to maintain adequate pain control (J. W. Kwan,
Am. J. Hosp. Pharm.
47 (Suppl 1):S18-23, 1990; J. S. Anulty,
International Anesthesiology Clinics
28:17-24, 1990; R. S. Sinatra,
The Yale Journal of Biology and Medicine
64:351-374, 1991. Continuous infusion or repetitive injections further necessitate placement of catheter systems with or without attached infusion pumps, all of which consume expensive physician and nursing time for care and maintenance. Furthermore, repeated bolus injections or continuous infusions can result in respiratory depression.
Late respiratory depression and apneic episodes are the side-effects of greatest concern in early studies (P. R. Bromage,
Anesthesia and Analgesia
60:461-463, 1981; E. M. Camporesi, et al.,
Anesthesia and Analgesia
62:633-640, 1983; T. L. Yaksh,
Pain
11:293-346, 1981). A recent prospective non-randomized study of epidural morphine in 1085 patients who have undergone thoracic, abdominal, or orthopedic surgeries estimated the rate of “respiratory depression” following epidural morphine to be 0.9% (R. Stenseth et al.,
Acta Anaesthesiol. Scand.
29:148-156, 1985). As a comparison, the incidence of “life-threatening respiratory depression” in 860 patients given systemic morphine (PO, IV, IM, SC) was 0.9% (R. R. Miller et al,
Drug Effects in Hospitalized Patients.
John Wiley & Sons, New York, 1976). Prospective, randomized studies comparing epidural opioid versus systemic opioids (IM or IV) in high risk patients have shown that postoperative pain control with epidural opioid results in superior analgesia with decreased incidence of post-operative complications (N. Rawal et al.,
Anesth. Analg.
63:583-592, 1984; M P. Yeager, et al.
Anesth.
60: 729-736, 1987).
The sustained release of various therapeutic agents after incorporation into liposomes, such as multivesicular liposomes, has been well documented both in vitro and in animals for intrathecal, subcutaneous, and intraperitoneal routes of administration, as well as in human patients for the intrathecal route of administration (S. Kim et al.,
J. Clin. Oncol.
11:2186-2193, 1993; V. Russack et al.,
Ann Neurol.
34:108-112, 1993; and M. C. Chamberlain et al.,
Arch. Neurol.
50:261-264, 1993). However, sustained release of epidurally administered compounds has heretofore been unknown in the art.
Therefore, the need exists for new and better methods for administering opioids and other therapeutic compounds epidurally as a single dose so as to achieve a sustained release rate at therapeutically effective levels. The present invention addresses the limitations of the prior art by providing a sustained-release formulation of a therapeutic agent such as an opioid, that results in maximal analgesia immediately after a single epidural dose and provides gradually decreasing analgesia over the next several days.


REFERENCES:
patent: 4078052 (1978-03-01), Papahadjopoulous
patent: 4089801 (1978-05-01), Schneider
patent: 4145410 (1979-03-01), Sears
patent: 4224179 (1980-09-01), Schneider
patent: 4235871 (1980-11-01), Papahadjopoulous et al.
patent: 4310506 (1982-01-01), Baldeschwieler et al.
patent: 4394372 (1983-07-01), Taylor
patent: 4522803 (1985-06-01), Lenk et al.
patent: 4588578 (1986-05-01), Fountain et al.
patent: 4599227 (1986-07-01), Dees et al.
patent: 4610868 (1986-09-01), Fountain et al.
patent: 4752425 (1988-06-01), Martin et al.
patent: 4769250 (1988-09-01), Forssen
patent: 4781871 (1988-11-01), West, III et al.
patent: 4788055 (1988-11-01), Fischer et al.
patent: 4816264 (1989-03-01), Phillips et al.
patent: 4828836 (1989-05-01), Elger et al.
patent: 4834965 (1989-05-01), Martani et al.
patent: 4834985 (1989-05-01), Elger et al.
patent: 4920016 (1990-04-01), Allen et al.
patent: 4921853 (1990-05-01), LeBlanc
patent: 4996047 (1991-02-01), Kelleher et al.
patent: 5000959 (1991-03-01), Iga et al.
patent: 5021200 (1991-06-01), Vanlerberghe et al.
patent: 5071646 (1991-12-01), Malkowska et al.
patent: 5077056 (1991-12-01), Bally et al.
patent: 5091187 (1992-02-01), Haynes
patent: 5091188 (1992-02-01), Haynes
patent: 5133974 (1992-07-01), Paradissis et al.
patent: 5204112 (1993-04-01), Hope et al.
patent: 5211955 (1993-05-01), Legros et al.
patent: 5227165 (1993-07-01), Domb et al.
patent: 5244678 (1993-09-01), Legros et al.
patent: 5246707 (1993-09-01), Haynes
patent: 5261903 (1993-11-01), Dhaliwal et al.
patent: 5321012 (1994-06-01), Mayer et al.
patent: 5451408 (1995-09-01), Mezei et al.
patent: 5459127 (1995-10-01), Felgner et al.
patent: RE35192 (1996-03-01), Reese
patent: 5612057 (1997-03-01), Lanza et al.
patent: 5922340 (1999-07-01), Berde et al.
patent: 5993850 (1999-11-01), Sankaram et al.
patent: 6132766 (2000-10-01), Sankaram et al.
patent: 0 280 503 (1988-08-01), None
patent: 2050287 (1981-01-01), None
patent: 2100030 (1990-04-01), None
patent: 2103994 (1991-07-01), None
patent: 2039043 (1992-06-01), None
patent: WO 89/10125 (1989-11-01), None
patent: WO 93/13128 (1993-07-01), None
patent: WO 95/13796 (1995-05-01), None
patent: WO 97/01351 (1997-01-01), None
Sinil Kim et al., “Multivesicular Liposomes Containing Cytarabine for Slow-Release Sc Administration,” Cancer Treatment Reports, vol. 71, No. 5, pp. 447-450, May 1987.
Sinil Kim et al., “Direct Cerebrospinal Fluid Delivery of an Antiretorviral Agent Using Multivesicular Liposomes,” Journal of Infectious Diseases, vol. 162, pp. 750-752, Sep. 1990.
Sinil Kim et al., “Multivesicular Liposomes containing 1-&bgr;-D-Arabinofuranosylcytosine for Slow-Release Intrathecal Therapy,” Cancer Research, vol. 47, pp. 3935-3937, Aug. 1, 1987.
Huang, “Studies of Phosphatidylcholine Vesicles Formation and Physical Characteristics,”Biochemistry,8:334-352, 1969.
Bangham, “Diffusion of Univalant Ions Across The Lamellae of Swollen Phospholipids,”J. Mol. Bio.,13:238-252, 1965.
Szoka, et al

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Epidural administration of therapeutic compounds with... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Epidural administration of therapeutic compounds with..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Epidural administration of therapeutic compounds with... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2902739

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.