IP Library › Granted Patent US 12,350,254
Granted Patent B2
US 12,350,254 · App. 17/666,216 · Granted Jul 8, 2025

Tumescent infiltration drug delivery of cannabinoids

Inventors: Jeffrey Alan Klein (San Juan Capistrano, CA); Paytra Alan Klein (Newport Beach, CA); Bram Alan Klein (Newport Beach, CA)
Assignee: HK TUMESCENT PHARMA
A61K31/352A61K9/0019A61K9/1075A61K31/137A61K31/522A61P23/02A61P31/20
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Quick Facts
Patent No.
US 12,350,254
App. No.
17/666,216
Granted
Jul 8, 2025
Kind
B2
Abstract

A tumescent composition including a cannabinoid dissolved in a tumescent solution, wherein the tumescent solution includes a local anesthetic; a vasoconstrictor; and a pharmaceutically acceptable carrier, wherein a tumescent concentration of the cannabinoid is 1-2000 μg/kg and is simultaneously: below a threshold for local, subcutaneous tissue toxicity, above a threshold for positive local therapeutic effect, and above a concentration safely achievable by intravenous (IV), intramuscular (IM) or oral (PO) delivery. Also disclosed are methods of subcutaneous delivery of a cannabinoid to a subject including administering to the subject the tumescent composition.

Claims (32)

1. A tumescent composition comprising a cannabinoid and a steroidal anti-inflammatory drug dissolved in a tumescent solution, wherein the tumescent solution comprises:

(i) a vasoconstrictor;

(ii) a pharmaceutically acceptable carrier; and

(iii) optionally a local anesthetic.

2. The tumescent composition of claim 1 , wherein the cannabinoid is a variant of cannabidiol (CBD) or tetrahydrocannabinol (THC).

3. The tumescent composition of claim 2 , wherein the cannabinoid is a variant of THC, wherein the alkyl side chain of thereof is derivatized.

4. The tumescent composition of claim 2 , wherein the cannabinoid is a variant of THC, wherein the phenolic hydroxyl group thereof is derivatized.

5. The tumescent composition of claim 1 , wherein the cannabinoid is an emulsion comprising CBD and/or THC.

6. The tumescent composition of claim 5 , wherein the emulsion is a micro- or nano-emulsion.

7. The tumescent composition of claim 1 , wherein said local anesthetic is lidocaine.

8. The tumescent composition of claim 7 , wherein the concentration of lidocaine is approximately 100 mg to 1,500 mg per L of solution.

9. The tumescent composition of claim 1 , wherein said vasoconstrictor component comprises epinephrine.

10. The tumescent composition of claim 9 , wherein the concentration of epinephrine is approximately 0.2 to 1.5 mg/L.

11. The tumescent composition according to claim 1 ,

wherein a tumescent concentration of the cannabinoid is 1-2000 μg/kg and is simultaneously:

1) Below a threshold for local, subcutaneous tissue toxicity,

2) Above a threshold for positive local therapeutic effect, and

3) Above a concentration safely achievable by intravenous (IV), intramuscular (IM) or oral (PO) delivery.

12. A method of subcutaneous delivery of a cannabinoid to a subject comprising administering to said subject the tumescent composition according to claim 1 .

13. The method of claim 12 , wherein infiltration of the tumescent composition achieves both prolonged local drug concentration within a tumescent subcutaneous tissue as well as a prolonged slow constant systemic absorption of drugs from the tumescent tissue into a systemic circulation.

14. The method of claim 12 , wherein a pharmacokinetic profile of the systemic absorption resembles a slow, constant, intravenous (IV) infusion.

15. The method of claim 12 , wherein the subcutaneous concentration of the cannabinoid and/or steroidal anti-inflammatory drug achieved is from about 1-100 times the maximum subcutaneous interstitial fluid concentration that can be achieved by conventional IV, IM or oral delivery of the cannabinoid.

16. The method of claim 12 , wherein said local anesthetic is lidocaine.

17. The method of claim 16 , wherein the concentration of lidocaine is approximately 100 mg to 1,500 mg per L of solution.

18. The method of claim 12 , wherein said vasoconstrictor component comprises epinephrine.

19. The method of claim 18 wherein the concentration of epinephrine is approximately 0.2 to 1.5 mg/L.

20. The method of claim 12 , wherein the subject is treated for a condition selected from the group consisting of surgically-induced neuropathic pain, shingles, inflammation, appetite loss, pain, multiple sclerosis, nausea, vomiting, and epilepsy.

21. A method of claim 20 , wherein said surgically-induced neuropathic pain results from breast cancer surgery, limb amputation, thoracotomy or hernia repair.

22. The method of claim 21 , wherein said breast cancer surgery is mastectomy or lumpectomy.

23. The method according to claim 12 , wherein the tumescent composition further comprises an antiviral drug.

24. The method according to claim 23 , wherein the antiviral drug is acyclovir.

25. The tumescent composition according to claim 1 , wherein the steroidal anti-inflammatory drug is triamcinolone.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 28, 2025
From: KLEIN, BRAM ALAN
To: HK TUMESCENT PHARMA
Reel/Frame 071237/0336 →
CHANGE OF NAME Recorded Dec 18, 2023
From: HK PHARMA
To: HK TUMESCENT PHARMA
Reel/Frame 066060/0356 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 8, 2022
From: KLEIN, JEFFREY ALAN; KLEIN, PAYTRA ALAN
To: HK PHARMA
Reel/Frame 058927/0292 →
Continuity (4)
Continuation 16264440 · Jan 31, 2019
Continuation In Part 15291417 · Oct 12, 2016
Provisional Application 62240439 · Oct 12, 2015
Related Publication 20220160677A1 · May 26, 2022
References Cited (33)
US 6248345B1 · Goldenheim et al. · 2001 [cited by applicant]
US 10493024B2 · Klein et al. · 2019 [cited by applicant]
US 11241412B2 · Klein et al. · 2022 [cited by applicant]
US 20020077437A1 · Silverberg et al. · 2002 [cited by applicant]
US 20020147238A1 · Jerussi et al. · 2002 [cited by applicant]
US 20030087962A1 · Demopulos et al. · 2003 [cited by applicant]
US 20050287134A1 · Klein · 2005 [cited by applicant]
US 20090098110A1 · Adams, Jr. et al. · 2009 [cited by applicant]
US 20110282271A1 · Klein · 2011 [cited by applicant]
US 20120195911A1 · Martynov et al. · 2012 [cited by applicant]
US 20120322783A1 · Klein · 2012 [cited by applicant]
US 20130116223A1 · Hexsel · 2013 [cited by applicant]
US 20130331313A1 · Berenson · 2013 [cited by applicant]
US 20150086494A1 · Sekura et al. · 2015 [cited by applicant]
US 20160030387A1 · Winnicki · 2016 [cited by applicant]
US 20160235851A1 · Sand et al. · 2016 [cited by applicant]
US 20170100331A1 · Klein et al. · 2017 [cited by applicant]
US 20170360772A1 · Bosse et al. · 2017 [cited by applicant]
US 20200237714A1 · Gabriele et al. · 2020 [cited by applicant]
EP 3917507 · 2021 [cited by applicant]
WO WO2010028288A2 · 2010 [cited by applicant]
WO WO2011066577A1 · 2011 [cited by applicant]
WO WO2018081740A1 · 2018 [cited by applicant]
WO WO2020160328A1 · 2020 [cited by applicant]
International Preliminary Report on patentability received in PCT/US2020/15963 on Aug. 12, 2021. [cited by applicant]
International Search Report and Written Opinion, PCT/US20/15963, mailed May 22, 2020. [cited by applicant]
Bruni, et al., “Cannabinoid Delivery Systems for Pain and Inflammation Treatment,” Molecules, 23, 2478, Sep. 27, 2018. [cited by applicant]
Klein, Jeffrey A., M.D., “Tumescent Technique for Local Anesthesia Improves Safety in Large-Volume Liposuction,” Plastic and Reconstructive Surgery, Nov. 1993. [cited by applicant]
Shany, Eilon, et al., “Comparison of Continuous Drip of Midazolam or Lidocaine in the Treatmnet of Intractable Neonatal Seizures,” Journalof Child Neurology, vol. 22, No. 3, Mar. 2007. [cited by applicant]
Gregg J M et al: “Cardiovascular effects of cannabinol during oral surgery”, Anesthesia and Analgesia 1976, vol. 55, No. 2, 1976, pp. 203-213. [cited by applicant]
Newton SC et al. “In vitro effects of psychoactive and non-psychoactive cannabinoids on immature rat Sertoli cell function” Life Sciences 1993;53(18):1429-1437. [cited by applicant]
Examination Report in corresponding European Application No. 20747957.7, dated Jul. 31, 2024 (in 8 pages). [cited by applicant]
Rehsia, N. S., & Dhalla, N. S. (2010). Potential of endothelin-1 and vasopressin antagonists for the treatment of congestive heart failure. Heart Failure Reviews, 15(1), 85-101. [cited by applicant]