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Evaluation of High-Performance Curcumin Nanocrystals for Pulmonary Drug Delivery Both In Vitro and In Vivo.

Hu L, Kong D, Hu Q, Gao N, Pang S - Nanoscale Res Lett (2015)

Bottom Line: The effects of different milling times on particle size and aerodynamic performance were investigated.Results showed that the drug dissolution was significantly enhanced by processing into curcumin-DPIs.The aerodynamic results indicated that the DPIs displayed a good aerosol performance.

View Article: PubMed Central - PubMed

Affiliation: School of Pharmaceutical Sciences, Hebei University, No. 180, WuSi Road, Baoding, 071002, People's Republic of China. hbupharm@126.com.

ABSTRACT
This paper focused on formulating high-performance curcumin spray-dried powders for inhalation (curcumin-DPIs) to achieve a high lung concentration. Curcumin-DPIs were produced using wet milling combined with the spray drying method. The effects of different milling times on particle size and aerodynamic performance were investigated. The curcumin-DPIs were characterized by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), and in vitro dissolution. Furthermore, the in vivo pharmacokinetic behavior and tissue distribution after pulmonary administration were also evaluated. Results showed that the drug dissolution was significantly enhanced by processing into curcumin-DPIs. The aerodynamic results indicated that the DPIs displayed a good aerosol performance. The plasma curcumin concentration was obviously enhanced by inhalation, and most of the curcumin-DPIs were deposited in the lung. This study demonstrated that inhalation was an effective way to carry drug to the lung, and curcumin-DPIs were hopeful for lung cancer treatment in the future.

No MeSH data available.


Related in: MedlinePlus

Particle sizes of unmilled bulk curcumin (0 min) and nanocrystals milled with different times
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Fig1: Particle sizes of unmilled bulk curcumin (0 min) and nanocrystals milled with different times

Mentions: The effects of milling time on particle sizes were shown in Fig. 1. For all cases, the concentration of Tween 80 was kept 6.25 % relative to the drug amount and the agitator speed was 3000 rpm. Before milling, the D50, D90, and D97 of bulk curcumin were 15.08, 47.19, and 75.01 μm, respectively.Fig. 1


Evaluation of High-Performance Curcumin Nanocrystals for Pulmonary Drug Delivery Both In Vitro and In Vivo.

Hu L, Kong D, Hu Q, Gao N, Pang S - Nanoscale Res Lett (2015)

Particle sizes of unmilled bulk curcumin (0 min) and nanocrystals milled with different times
© Copyright Policy - OpenAccess
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC4591223&req=5

Fig1: Particle sizes of unmilled bulk curcumin (0 min) and nanocrystals milled with different times
Mentions: The effects of milling time on particle sizes were shown in Fig. 1. For all cases, the concentration of Tween 80 was kept 6.25 % relative to the drug amount and the agitator speed was 3000 rpm. Before milling, the D50, D90, and D97 of bulk curcumin were 15.08, 47.19, and 75.01 μm, respectively.Fig. 1

Bottom Line: The effects of different milling times on particle size and aerodynamic performance were investigated.Results showed that the drug dissolution was significantly enhanced by processing into curcumin-DPIs.The aerodynamic results indicated that the DPIs displayed a good aerosol performance.

View Article: PubMed Central - PubMed

Affiliation: School of Pharmaceutical Sciences, Hebei University, No. 180, WuSi Road, Baoding, 071002, People's Republic of China. hbupharm@126.com.

ABSTRACT
This paper focused on formulating high-performance curcumin spray-dried powders for inhalation (curcumin-DPIs) to achieve a high lung concentration. Curcumin-DPIs were produced using wet milling combined with the spray drying method. The effects of different milling times on particle size and aerodynamic performance were investigated. The curcumin-DPIs were characterized by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), and in vitro dissolution. Furthermore, the in vivo pharmacokinetic behavior and tissue distribution after pulmonary administration were also evaluated. Results showed that the drug dissolution was significantly enhanced by processing into curcumin-DPIs. The aerodynamic results indicated that the DPIs displayed a good aerosol performance. The plasma curcumin concentration was obviously enhanced by inhalation, and most of the curcumin-DPIs were deposited in the lung. This study demonstrated that inhalation was an effective way to carry drug to the lung, and curcumin-DPIs were hopeful for lung cancer treatment in the future.

No MeSH data available.


Related in: MedlinePlus