
A new review by a team of researchers from Indonesia, Japan and China, led by Professor Nurhasni Hasan from the Faculty of Pharmacy at Hasanuddin University in Indonesia, examines how emerging local drug delivery systems could be designed to overcome barriers to treating oral squamous cell carcinoma (OSCC), which is one of the most common malignancies affecting the oral cavity and head and neck region and contributes significantly to the global burden of cancer-related morbidity and mortality.
Treating oral cancer with drugs delivered directly to the lesion site is a promising approach. This requires that the medicine remain at the cancer site long enough to provide sustained treatment, increasing drug exposure to the tumor while reducing unwanted exposure throughout the body. But there is a fundamental challenge: The mouth is constantly working against the medicine, creating what the authors describe as stringent “hard constraints” for effective local drug delivery. Saliva can dilute and wash away medicines, while enzymes, chewing, speaking and tongue movement can degrade or dislodge drug-delivery systems used for treatment.
The review was published in the European Journal of Pharmaceutics and Biopharmaceutics on Aug. 1, 2026. It brings together different approaches to local OSCC treatment, including mucoadhesive films and patches, oral sprays, in situ gels and injectable hydrogels. Rather than treating these technologies as one-size-fits-all solutions, the researchers emphasize that the best delivery system may depend on the characteristics of both the drug and the tumor.
“There is a tendency to think of drug delivery as a problem that can be solved by developing a better formulation,” Hasan said. “However, the bigger question is whether the formulation is appropriate for that particular clinical situation.”
Depending on its shape and location, a flat, accessible lesion would be suitable for mucoadhesive films that remain attached to the mucosa while delivering the drug. However, irregular or infiltrative lesions may benefit from gels or injectable hydrogels that can conform to complex tissue surfaces and provide more sustained drug exposure by delivering the drug to deeper layers. Sprays are comparatively convenient to apply but have shorter residence times because of salivary clearance.
Moreover, the oral environment also undergoes changes during cancer treatment. Radiotherapy and chemotherapy often result in xerostomia, or dry mouth, and mucosal damage, affecting hydration, lubrication, drug release and adhesion. An increase in salivary flow leads to accelerated dilution and clearance, indicating that formulations tested under simplified laboratory conditions may not perform the same way in patients.
The researchers state that a more realistic evaluation of local drug-delivery systems is required. They emphasize that future studies should focus on how well formulations remain attached under salivary flow and mechanical stress, maintain stability amid changes in pH and enzymatic activity, and deliver drugs consistently to tumor margins. Additionally, the review assessed the translational maturity of different types of formulations.
“A sophisticated technology has limited clinical value if it is difficult to manufacture, administer or tolerate. These practical considerations must guide formulation development from the start,” Hasan said.
Mucoadhesive films and patches currently appear to have stronger near-term potential because similar buccal delivery formats already have regulatory and manufacturing precedents Injectable hydrogels, on the other hand, offer promising options for irregular lesions but face additional challenges involving manufacturing, gelation, degradation, clinical application and long-term biocompatibility.
Notably, these technologies are not yet established treatments for OSCC. The review provides a framework for moving promising approaches toward clinical use by matching the delivery system to the drug, tumor and conditions experienced by each individual patient.
Taken together, the researchers suggest that the next generation of local oral cancer therapies should be designed to keep the right amount of drug at the right place for the right length of time, not merely to deliver drugs. “The goal should be to make local treatment more predictable. We need delivery systems that researchers can evaluate consistently and clinicians can realistically use,” Hasan concluded.
More information
Muhammad Ruslin et al, Local drug delivery for oral squamous cell carcinoma under oral cavity, European Journal of Pharmaceutics and Biopharmaceutics (2026). DOI: 10.1016/j.ejpb.2026.115114
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Rethinking oral cancer treatment: A review of next-generation drug delivery systems (2026, August 26)
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