Improved transdermal delivery of novel cannabinoid-loaded patches using Eudragit matrix

被引:1
|
作者
Wongwad, Eakkaluk [1 ]
Ingkaninan, Kornkanok [2 ,3 ]
Waranuch, Neti [3 ,4 ]
Park, Chulhun [5 ]
Somayaji, Vijay [6 ]
Na-Ek, Nat [7 ]
Lobenberg, Raimar [6 ]
机构
[1] Univ Phayao, Sch Pharmaceut Sci, Dept Cosmet Sci, Phayao 56000, Thailand
[2] Naresuan Univ, Fac Pharmaceut Sci, Dept Pharmaceut Chem & Pharmacognosy, Bioscreening Unit, Phitsanulok 65000, Thailand
[3] Naresuan Univ, Ctr Excellence Innovat Chem, Phitsanulok 65000, Thailand
[4] Naresuan Univ, Fac Pharmaceut Sci, Cosmet & Nat Prod Res Ctr, Dept Pharmaceut Technol, Phitsanulok 65000, Thailand
[5] Jeju Natl Univ, Coll Pharm, Jeju 63243, South Korea
[6] Univ Alberta, Fac Pharm & Pharmaceut Sci, Edmonton, AB T6G 2E1, Canada
[7] Univ Phayao, Sch Pharmaceut Sci, Dept Pharmaceut Care, Div Social & Adm Pharm, Phayao, Thailand
关键词
Cannabinoids; CBDA; Stability; Transdermal patch; THCA; Eudragit (R) E100; PERMEATION ENHANCERS; SKIN PERMEATION; DRUG-DELIVERY; CANNABIDIOLIC ACID; FORMULATION; VIVO; OPTIMIZATION; MICRONEEDLES; RELEASE; GEL;
D O I
10.1016/j.jddst.2024.105697
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The main active cannabinoids in extracts of Cannabis sativa L., cannabidiolic acid (CBDA) and tetrahydrocannabinolic acid (THCA), are known for their pharmacological effects, including anti-inflammatory, analgesic, psychedelic, anti-cancer, and anti-spasmodic activities. This study aimed to develop adhesive cannabinoidloaded transdermal patches (CLTPs) to enhance the skin permeation of the active cannabinoids, CBDA and THCA, and evaluate their stability. Optimized CLTPs were prepared in 1.5 % (w/w) polyvinyl alcohol-coated petri dishes using a solvent casting technique. The casting solution consisted of mixtures of isopropyl alcohol and ethanol, along with Eudragit (R) E100, succinic acid, dibutyl phthalate, and permeation enhancers such as oleic acid, isopropyl myristate, mixtures of oleic acid and isopropyl myristate, ethoxydiglycol, sesame oil, and copolymer (Kollidon (R) VA64). The physicochemical properties of the patches were characterized by uniformity, thickness, drug content, swelling, and mechanical properties. The in vitro release studies of CBDA and THCA through a synthetic hydrophobic membrane using various release enhancers from these patches were conducted using Franz diffusion cells. Using ethoxydiglycol as a release enhancer demonstrated the highest release profile for both cannabinoids. The steady-state flux values of CBDA and THCA were 3.83 +/- 0.45 mu g/cm2/h (1.85-fold compared to the control) and 0.72 +/- 0.14 mu g/cm2/h (1.54-fold compared to the control) at 8 h. The stability studies of CLTPs demonstrated that both remained stable at 4 degrees C for at least 90 days. In conclusion, transdermal patches containing cannabinoids have been successfully developed and characterized. These findings offer a promising avenue for further investigation of CLTPs, as they could serve as a versatile formulation strategy for pharmaceutical products.
引用
收藏
页数:10
相关论文
共 50 条
  • [1] Development of a novel cannabinoid-loaded microemulsion towards an improved stability and transdermal delivery
    Park, Chulhun
    Zuo, Jieyu
    Somayaji, Vijay
    Lee, Beom-Jin
    Lobenberg, Raimar
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2021, 604
  • [2] Enhancement of transdermal delivery of resveratrol using Eudragit and polyvinyl pyrrolidone-based dissolving microneedle patches
    Aung, Nway Nway
    Ngawhirunpat, Tanasait
    Rojanarata, Theerasak
    Patrojanasophon, Prasopchai
    Opanasopit, Praneet
    Pamornpathomkul, Boonnada
    JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY, 2021, 61
  • [3] Combination of transdermal patches and solid microneedles for improved transdermal delivery of primaquine
    Ananda, Putri Wulandari Resky
    Elim, Diany
    Zaman, Hilman Syamami
    Muslimin, Wahdaniyah
    Tunggeng, Muhamad Gilang Ramadhan
    Permana, Andi Dian
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2021, 609
  • [4] Adhesion testing of polyurethane matrix patches for transdermal delivery of testosterone
    Dittgen, M.
    Gansen, P.
    PHARMAZIE, 2012, 67 (06): : 567 - 568
  • [5] Development of matrix patches for transdermal delivery of a highly lipophilic antiestrogen
    Funke, AP
    Günther, C
    Müller, RH
    Lipp, R
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2003, 29 (07) : 785 - 793
  • [6] Local Delivery of Cannabinoid-Loaded Microparticles Inhibits Tumor Growth in a Murine Xenograft Model of Glioblastoma Multiforme
    Hernan Perez de la Ossa, Dolores
    Lorente, Mar
    Esther Gil-Alegre, Maria
    Torres, Sofia
    Garcia-Taboada, Elena
    del Rosario Aberturas, Maria
    Molpeceres, Jesus
    Velasco, Guillermo
    Isabel Torres-Suarez, Ana
    PLOS ONE, 2013, 8 (01):
  • [7] Fabrication and characterization of matrix type transdermal patches loaded with tizanidine hydrochloride: potential sustained release delivery system
    Shahid, Nabeel
    Siddique, Muhammad Irfan
    Razzaq, Zunera
    Katas, Haliza
    Waqas, Muhammad Khurram
    Kashif-Ur-Rahman
    DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2018, 44 (12) : 2061 - 2070
  • [8] DEVELOPMENT AND EVALUATION OF MATRIX PATCHES AS TRANSDERMAL DRUG DELIVERY SYSTEM FOR AMLODIPINE
    Abrar, Muhammad Asad
    Ahmad, Mahmood
    Akram, Muhammad Rouf
    ACTA POLONIAE PHARMACEUTICA, 2018, 75 (01): : 119 - 127
  • [9] Fabrication of Tizanidine Loaded Patches Using Flaxseed Oil and Coriander Oil as a Penetration Enhancer for Transdermal Delivery
    Akhlaq, Muhammad
    Azad, Abul Kalam
    Fuloria, Shivkanya
    Meenakshi, Dhanalekshmi Unnikrishnan
    Raza, Sajid
    Safdar, Muhammad
    Nawaz, Asif
    Subramaniyan, Vetriselvan
    Sekar, Mahendran
    Sathasivam, Kathiresan V.
    Wu, Yuan Seng
    Miret, Mireia Mallandrich
    Fuloria, Neeraj Kumar
    POLYMERS, 2021, 13 (23)
  • [10] Pharmacokinetics of a New Fentanyl Tape with a Novel Delivery System of Transdermal Matrix Patches in Patients with Cancer Pain
    Saito, Takefumi
    Fujii, Masato
    Saito, Shiro
    Shimada, Ken
    Fujiwara, Keiichi
    Kobayashi, Kunihiko
    ONCOLOGY, 2014, 86 (01) : 10 - 15