Preparation and Evaluation of Directly Compressible Orally Disintegrating Tablets of Cannabidiol Formulated Using Liquisolid Technique

This study demonstrated the implementation of a liquisolid technique to formulate directly compressible orally disintegrating tablets (ODTs). Cannabidiol (CBD), a hydrophobic cannabinoid, was prepared as a liquisolid powder using microcrystalline cellulose–colloidal silicon dioxide as a carrier–coat...

Full description

Bibliographic Details
Main Authors: Ekapol Limpongsa, Peera Tabboon, Thaned Pongjanyakul, Napaphak Jaipakdee
Format: Article
Language:English
Published: MDPI AG 2022-11-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/14/11/2407
_version_ 1797466845863739392
author Ekapol Limpongsa
Peera Tabboon
Thaned Pongjanyakul
Napaphak Jaipakdee
author_facet Ekapol Limpongsa
Peera Tabboon
Thaned Pongjanyakul
Napaphak Jaipakdee
author_sort Ekapol Limpongsa
collection DOAJ
description This study demonstrated the implementation of a liquisolid technique to formulate directly compressible orally disintegrating tablets (ODTs). Cannabidiol (CBD), a hydrophobic cannabinoid, was prepared as a liquisolid powder using microcrystalline cellulose–colloidal silicon dioxide as a carrier–coating material. Different liquid vehicles differing in their volatility, hydrophilicity, and viscosity were investigated. Each of the CBD–ODTs comprised CBD liquisolid powder (10 mg CBD), superdisintegrant, flavors, lubricant, and filler. The physical mixture (PM) ODT was prepared as a control. Ethanol-based ODTs (CBD–EtOH–ODTs) had comparable tablet properties and stability to CBD–PM–ODTs. ODTs with nonvolatile-vehicle-based liquisolid powder had lower friability but longer disintegration times as compared with CBD–PM–ODTs and CBD–EtOH–ODTs. Compression pressure influenced the thickness, hardness, friability, and disintegration of the ODTs. With a suitable compression pressure to yield 31-N-hardness-ODTs and superdisintegrant (4–8%), CBD–ODTs passed the friability test and promptly disintegrated (≤25 s). Times to dissolve 50% of CBD–PM–ODTs, CBD–EtOH–ODTs, and nonvolatile-vehicle-based CBD–ODTs were 10.1 ± 0.7, 3.8 ± 0.2, and 4.2 ± 0.4–5.0 ± 0.1 min, respectively. CBD–EtOH–ODTs exhibited the highest dissolution efficiency of 93.5 ± 2.6%. Long-term and accelerated storage indicated excellent stability in terms of tablet properties and dissolution. Nonvolatile-vehicle-based CBD–ODTs exhibited a higher percentage of remaining CBD. This study provides useful basic information for the development of ODT formulations using a liquisolid technique application.
first_indexed 2024-03-09T18:45:27Z
format Article
id doaj.art-d4955f3953e44031b05561fc58fde74e
institution Directory Open Access Journal
issn 1999-4923
language English
last_indexed 2024-03-09T18:45:27Z
publishDate 2022-11-01
publisher MDPI AG
record_format Article
series Pharmaceutics
spelling doaj.art-d4955f3953e44031b05561fc58fde74e2023-11-24T06:21:46ZengMDPI AGPharmaceutics1999-49232022-11-011411240710.3390/pharmaceutics14112407Preparation and Evaluation of Directly Compressible Orally Disintegrating Tablets of Cannabidiol Formulated Using Liquisolid TechniqueEkapol Limpongsa0Peera Tabboon1Thaned Pongjanyakul2Napaphak Jaipakdee3College of Pharmacy, Rangsit University, Pathum Thani 12000, ThailandDivision of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, ThailandDivision of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, ThailandDivision of Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen 40002, ThailandThis study demonstrated the implementation of a liquisolid technique to formulate directly compressible orally disintegrating tablets (ODTs). Cannabidiol (CBD), a hydrophobic cannabinoid, was prepared as a liquisolid powder using microcrystalline cellulose–colloidal silicon dioxide as a carrier–coating material. Different liquid vehicles differing in their volatility, hydrophilicity, and viscosity were investigated. Each of the CBD–ODTs comprised CBD liquisolid powder (10 mg CBD), superdisintegrant, flavors, lubricant, and filler. The physical mixture (PM) ODT was prepared as a control. Ethanol-based ODTs (CBD–EtOH–ODTs) had comparable tablet properties and stability to CBD–PM–ODTs. ODTs with nonvolatile-vehicle-based liquisolid powder had lower friability but longer disintegration times as compared with CBD–PM–ODTs and CBD–EtOH–ODTs. Compression pressure influenced the thickness, hardness, friability, and disintegration of the ODTs. With a suitable compression pressure to yield 31-N-hardness-ODTs and superdisintegrant (4–8%), CBD–ODTs passed the friability test and promptly disintegrated (≤25 s). Times to dissolve 50% of CBD–PM–ODTs, CBD–EtOH–ODTs, and nonvolatile-vehicle-based CBD–ODTs were 10.1 ± 0.7, 3.8 ± 0.2, and 4.2 ± 0.4–5.0 ± 0.1 min, respectively. CBD–EtOH–ODTs exhibited the highest dissolution efficiency of 93.5 ± 2.6%. Long-term and accelerated storage indicated excellent stability in terms of tablet properties and dissolution. Nonvolatile-vehicle-based CBD–ODTs exhibited a higher percentage of remaining CBD. This study provides useful basic information for the development of ODT formulations using a liquisolid technique application.https://www.mdpi.com/1999-4923/14/11/2407cannabinoidsdisintegrating tabletsorodispersible tabletsliquid vehiclesdissolution enhancement
spellingShingle Ekapol Limpongsa
Peera Tabboon
Thaned Pongjanyakul
Napaphak Jaipakdee
Preparation and Evaluation of Directly Compressible Orally Disintegrating Tablets of Cannabidiol Formulated Using Liquisolid Technique
Pharmaceutics
cannabinoids
disintegrating tablets
orodispersible tablets
liquid vehicles
dissolution enhancement
title Preparation and Evaluation of Directly Compressible Orally Disintegrating Tablets of Cannabidiol Formulated Using Liquisolid Technique
title_full Preparation and Evaluation of Directly Compressible Orally Disintegrating Tablets of Cannabidiol Formulated Using Liquisolid Technique
title_fullStr Preparation and Evaluation of Directly Compressible Orally Disintegrating Tablets of Cannabidiol Formulated Using Liquisolid Technique
title_full_unstemmed Preparation and Evaluation of Directly Compressible Orally Disintegrating Tablets of Cannabidiol Formulated Using Liquisolid Technique
title_short Preparation and Evaluation of Directly Compressible Orally Disintegrating Tablets of Cannabidiol Formulated Using Liquisolid Technique
title_sort preparation and evaluation of directly compressible orally disintegrating tablets of cannabidiol formulated using liquisolid technique
topic cannabinoids
disintegrating tablets
orodispersible tablets
liquid vehicles
dissolution enhancement
url https://www.mdpi.com/1999-4923/14/11/2407
work_keys_str_mv AT ekapollimpongsa preparationandevaluationofdirectlycompressibleorallydisintegratingtabletsofcannabidiolformulatedusingliquisolidtechnique
AT peeratabboon preparationandevaluationofdirectlycompressibleorallydisintegratingtabletsofcannabidiolformulatedusingliquisolidtechnique
AT thanedpongjanyakul preparationandevaluationofdirectlycompressibleorallydisintegratingtabletsofcannabidiolformulatedusingliquisolidtechnique
AT napaphakjaipakdee preparationandevaluationofdirectlycompressibleorallydisintegratingtabletsofcannabidiolformulatedusingliquisolidtechnique