TY - JOUR
T1 - Hybrid Nanoparticles Dual-Loaded With Curcumin and Benzydamine Hydrochloride for the Treatment of Vulvovaginal Candidiasis
T2 - From Development to Biological Application In Vitro and In Vivo
AU - Carvalho, Gabriela C.
AU - Domingues, Maria Nolasco Viseu
AU - Marena, Gabriel Davi
AU - Mäkilä, Ermei
AU - Li, Jiachen
AU - Geertsema-Doornbusch, Gésinda
AU - de Andrade, Cleverton Roberto
AU - Stuart, Marc C. A.
AU - Shahbazi, Mohammad-Ali
AU - Corrêa, Ione
AU - Peterson, Brandon W.
AU - Salonen, Jarno
AU - Florindo, Helena F.
AU - Bauab, Taís Maria
AU - Chorilli, Marlus
AU - Santos, Hélder A.
PY - 2024/9/27
Y1 - 2024/9/27
N2 - Abstract Vulvovaginal candidiasis represents a public health challenge due to its reports of high incidence and recurrence. These are caused by host-related factors like compromised immune system, or pathogen-related factors, such as resistance to antifungal agents, making this medical problem desirable to develop new therapeutic options. In this context, natural origin substances like curcumin, are increasingly treatment alternatives. However, some curcumin properties limit its therapeutic application, such as insolubility in aqueous solvents, which leads to low bioavailability. Nevertheless, nanotechnology association with drugs of plant origin proves to be a promising alternative to overcome the reported drawbacks. Despite being caused by a fungus, patients suffer significantly from the inflammation resulting from this disease, thus this study aimed to develop a hybrid carrier nanoformulation by microfluidics loaded with two drugs, benzydamine hydrochloride (an anti-inflammatory drug) and curcumin (an antifungal drug). Transmission electron cryomicroscopy combined with energy dispersive X-ray analysis confirmed that the nanoparticle is properly developed. Through in vitro biological studies, it is possible to observe that, in addition to being safe, the encapsulation of both drugs in the nanocarrier drastically reduced their cytotoxicity. Finally, although the final nanoformulation does not show in vitro activity, the in vivo study indicated therapeutic potential.
AB - Abstract Vulvovaginal candidiasis represents a public health challenge due to its reports of high incidence and recurrence. These are caused by host-related factors like compromised immune system, or pathogen-related factors, such as resistance to antifungal agents, making this medical problem desirable to develop new therapeutic options. In this context, natural origin substances like curcumin, are increasingly treatment alternatives. However, some curcumin properties limit its therapeutic application, such as insolubility in aqueous solvents, which leads to low bioavailability. Nevertheless, nanotechnology association with drugs of plant origin proves to be a promising alternative to overcome the reported drawbacks. Despite being caused by a fungus, patients suffer significantly from the inflammation resulting from this disease, thus this study aimed to develop a hybrid carrier nanoformulation by microfluidics loaded with two drugs, benzydamine hydrochloride (an anti-inflammatory drug) and curcumin (an antifungal drug). Transmission electron cryomicroscopy combined with energy dispersive X-ray analysis confirmed that the nanoparticle is properly developed. Through in vitro biological studies, it is possible to observe that, in addition to being safe, the encapsulation of both drugs in the nanocarrier drastically reduced their cytotoxicity. Finally, although the final nanoformulation does not show in vitro activity, the in vivo study indicated therapeutic potential.
KW - benzydamine hydrochloride
KW - curcumin
KW - lipids
KW - mesoporous silica nanoparticles
KW - thermo-responsive hydrogel
KW - vulvovaginal candidiasis
U2 - 10.1002/adtp.202400342
DO - 10.1002/adtp.202400342
M3 - Article
SN - 2366-3987
JO - Advanced Therapeutics
JF - Advanced Therapeutics
M1 - 2400342
ER -