Submitted:
01 December 2025
Posted:
02 December 2025
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Abstract
Industrial hemp flower oil has gained attention in the nutraceutical field for its anti-inflammatory properties beneficial to skin health, particularly in acne management. The primary objective of this review is to evaluate whether hemp-derived compounds, especially cannabidiol (CBD), can effectively reduce inflammatory lesions, modulate cytokine activity and reduce acne severity while maintaining safety and tolerability. Acne vulgaris is characterised by inflammation, sebaceous gland hyperactivity and microbial colonisation, with evidence suggesting that CBD and hemp flower extracts down-regulate pro-inflammatory cytokines such as TNF-α, IL-1β, and IL-8. Methods reported in clinical studies include twice-daily topical application of hemp oil formulations, assessed through lesion counts and inflammatory markers over several weeks. Results consistently demonstrate reductions in inflammatory lesions, decreased sebum production and inhibition of Cutibacterium acnes growth, alongside favourable tolerability profiles. These findings indicate that hemp flower oil offers multi-targeted effects addressing key pathological factors such as inflammation, oxidative stress and sebocyte activity. Conclusively, industrial hemp flower oil emerges as a promising natural anti-inflammatory nutraceutical for acne management; however, large-scale randomised clinical trials are needed to standardise formulations and confirm long-term efficacy and safety across diverse populations.
Keywords:
1. Introduction
Primary Objective
- To synthesise current evidence on the efficacy and sustainability of industrial hemp flower oil and its derivatives as nutraceutical agents for skin health, with a focus on acne management.
Specific Objectives
- Evaluate current evidence on the anti-inflammatory and antimicrobial properties of hemp-derived compounds (e.g., cannabidiol and hemp seed oil) in acne treatment.
- Determine the efficacy of topical hemp-based formulations in reducing acne severity and targeting key pathogenic factors such as pro-inflammatory cytokines, lipid overproduction and microbial colonisation (Cutibacterium acnes).
- Identify gaps in standardisation regarding CBD concentrations, formulation stability and dosage guidelines for therapeutic use.
- Assess the extent of antimicrobial activity of CBD and hemp extracts, including variations in efficacy and optimal concentrations for clinical application.
- Explore sustainability and resilience within the hemp supply chain, focusing on eco-friendly cultivation and processing practices aligned with SDG 3 (Good health and Wellbeing).
- Examine the integration of nutraceuticals into dermatological practice as a sustainable alternative to conventional acne treatments.
Review Questions
- What evidence supports the anti-inflammatory and antimicrobial properties of industrial hemp flower oil and its derivatives in acne management?
- How do hemp-based formulations influence key pathogenic factors such as cytokine activity, lipid production, and Cutibacterium acnes proliferation?
- What are the reported optimal concentrations and formulation strategies for achieving therapeutic efficacy?
- What inconsistencies or limitations exist in current research regarding CBD’s antimicrobial activity and clinical outcomes?
- How can sustainable and resilient hemp supply chains contribute to the accessibility and safety of nutraceutical-based skin health solutions?
- In what ways do hemp-derived nutraceuticals align with global health and sustainability goals, particularly SDG 3?
2. Materials and Methods
- Records identified: 245
- Records screened: 245
- Records excluded: 190
- Full-text articles assessed for eligibility: 55
- Full-text articles excluded: 35
- Studies included in qualitative synthesis: 20
3. Results
3.1. Overview of Study Selection and Characteristics
3.2. Industrial Hemp Flower Oil and Anti-Inflammatory Properties
3.2.1. Nutraceuticals Role in Skin Health
3.2.1.1. Nanoformulation Advances
3.2.1.2. Phytochemical Diversity and Bioactivity
3.2.1.3. Sustainability and Supply Chain Resilience
3.2.1.4. Safety, Regulation and Evidence Gaps
3.3. Cannabidiol (CBD) as a Bioactive Compound
3.4. Sebum Regulation
3.5. Cutibacterium Acnes Suppression
3.6. Skin Inflammation Mitigation
3.7. Fatty Acids Contribution
3.8. Topical Application Approaches
3.9. Sustainability in Hemp Production
3.10. Resilience of Industrial Hemp Supply Chain
4. Discussion
5. Conclusions
Author Contributions
Funding
Acknowledgments
Conflicts of Interest
Abbreviations
| CBD | Cannabidiol |
| THC | Tetrahydrocannabinol |
| CB₁ | Cannabinoid Receptor Type 1 |
| CB₂ | Cannabinoid Receptor Type 2 |
| TRPV1 | Transient Receptor Potential Vanilloid 1 |
| TRPV4 | Transient Receptor Potential Vanilloid 4 |
| TNF-α | Tumour Necrosis Factor Alpha |
| IL-1β | Interleukin 1 Beta |
| IL-6 | Interleukin 6 |
| IL-8 | Interleukin 8 |
| PPARγ | Peroxisome Proliferator-Activated Receptor Gamma |
| ECS | Endocannabinoid System |
| NF-κB | Nuclear Factor Kappa-Light-Chain-Enhancer of Activated B Cells |
| MAPK | Mitogen-Activated Protein Kinase |
| RCT | Randomised Controlled Trial |
| PRISMA | Preferred Reporting Items for Systematic Reviews and Meta-Analyses |
| PROSPERO | International Prospective Register of Systematic Reviews |
| SDG | Sustainable Development Goal |
| NLC | Nanostructured Lipid Carrier |
| ROS | Reactive Oxygen Species |
| PUFAs | Polyunsaturated Fatty Acids |
| RHS | Responsible Hemp Standard |
| WHO | World Health Organization |
| BMJ | British Medical Journal |
| PLoS ONE | Public Library of Science ONE |
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| Reference | Study Type | Formulation Details | Protocol | Key Results | Reference |
| 1 | In vitro | CBD solution 1 and 10 μM | Single and sustained application on sebocytes, 14 days | Reduced sebocyte proliferation and lipogenesis; 50 μM dose induced cytotoxicity; strong anti-inflammatory effects | [68] |
| 2 | In vivo | Cream with 3% cannabis seed extract | 11 men, twice daily application for 3 months | 11.4% decrease in erythema with CBD cream vs. 4.3% control; 38% sebum reduction with CBD vs. 15% control; no irritation | [69] |
| 3 | In vitro | CBD 0.5-2 μM on human epidermal keratinocytes | Applied to cells stimulated by C acnes vesicles |
Downregulated inflammatory cytokines IL-6, IL-8, TNF-α; upregulated CB2 receptor expression | [70] |
| 4 | In vivo | Gel: 1% CBD, 1% Centella asiatica, 1% silymarin, 0.5% salicylic acid | 30 subjects, mild-moderate acne, 2-3 times daily, 56 days | 70.9% reduction in acne lesions, especially inflammatory ones | [16] |
| 5 | In vitro | CBD in DMSO at 10 μM | Tested on 3D sebocyte gland model and macrophages, 24h | Significant reduction in reactive oxygen species (ROS); decreased inflammatory macrophage marker CD86 | [71] |
| Reference | Adverse events reported | Safety commentary |
| [9] | None significant | Good short-term safety profile |
| [10] | No serious adverse events | Tolerability confirmed |
| [1] | Not reported | Safety considered acceptable |
| [72] | No serious adverse events | Long-term safety remains unverified |
| Nanoformulation Type | Mechanism | Observed Benefit | Reference |
| Liposomal CBD | Encapsulation within phospholipid bilayers | Enhanced skin penetration and hydration | [1] |
| Nanostructured Lipid Carrier (NLC) Gel | Co-loaded lipid system | Sustained release, reduced irritation | [2] |
| CBD-Capped Inorganic Nanoparticles | Metallic nanoparticle surface modification | Synergistic anti-inflammatory and antimicrobial effects | [3] |
| Hybrid Nanoemulsions | Colloidal hybrid stabilisers | Improved epidermal permeation and wound healing | [3] |
| Compound Class | Key Examples | Reported Function | Evidence Strength |
| Cannabinoids | CBD, CBG, CBC, THCV | Anti-inflammatory, sebostatic | High (clinical and preclinical) |
| Terpenes | β-caryophyllene, limonene | Antioxidant, antimicrobial | Moderate |
| Polyphenols | Cannflavin A, lignanamides | Antioxidant, anti-inflammatory | Moderate |
| Fatty Acids | Linoleic, α-linolenic acids | Skin barrier repair, hydration | High |
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