In addition, this cancer is difficult to treat because it typically develops from

liver cirrhosis and high rates of liver cancer recurrence and metastasis occur even after clinical HKI-272 datasheet diagnosis and treatment. Due to various issues, such as lack of specific treatments, limited innovative medications, and dearth of therapeutic options, it is particularly important and urgent to develop new techniques and therapies for diagnosis and treatment of liver cancer [3]. Photodynamic therapy (PDT), a new method developed during the past 2 decades for the treatment of malignant tumors, has shown good therapeutic effects on a variety of solid tumors [4, 5]. However, relatively few studies have been conducted to test whether this therapy can be used for hepatic and other intraperitoneal tumors. PDT involves two processes: (1) light sensitivity is achieved by the administration of photosensitizers to patients

and (2) light Sorafenib is transmitted through an optical fiber to the region of the body containing the tumor. Irradiation with light of appropriate wavelength will see more activate the photosensitizer, which transfers energy to oxygen, triggering a series of reactions leading to cell apoptosis or necrosis. Therefore, photosensitizers play a key role in PDT. Conventional PDT efficacy is restricted by insufficient selectivity, low solubility of photosensitizers, and limited penetration depth of the 630-nm laser light, which reduces the PDT efficacy for tumors located in deeper tissues compared with those at the body surface. In order to improve the photodynamic efficacy, a photosensitizer with high permeability and low side effects must be provided [6, 7], which allows concentrations to reach the required level for PDT. Recent progress in nanopharmaceutical research has proposed a few methods to tackle these

problems [8]. Researchers Olopatadine have developed various types of nanoscale drug carriers to deliver photosensitizers, such as liposomes [4, 5], polymer carriers [9], polyoxyethylene cremophor emulsions [10], and microspheres and nanoparticles [11]. Although these carriers improve photosensitizer properties, their use necessarily involves processes to release the loaded drugs that decrease the rate at which tumor cells absorb photosensitizers, extending the period of time required to reach effective concentrations [12]. Therefore, the development of nanocarriers that do not require an extensive process for releasing loaded photosensitizers would greatly enhance photosensitizer effectiveness by shortening this time period. Because nanoparticles are ideal carriers of photosensitizers [13], the use of silica nanoparticles as carriers for photosensitizers is an extremely viable option [14]. In this study, we aimed to compare the inhibitory effects of photosensitizers loaded in hollow silica nanoparticles and conventional photosensitizers on HepG2 human hepatoma cell proliferation and determine the underlying mechanisms in vitro.