TY - JOUR
T1 - Improved Iron Uptake and Metabolism Through Combined Heme and Non-Heme Iron Supplementation: An In Vitro Study
AU - Parini, Francesca
AU - Galla, Rebecca
AU - Mulè, Simone
AU - Musu, Matteo
AU - UBERTI, FRANCESCA
PY - 2025
Y1 - 2025
N2 - Iron is essential for numerous physiological processes, including oxygen transport, energy
metabolism, and immune function. This study evaluated the efficacy and safety of three iron
formulations combining heme and non-heme iron, comparing them with existing market
products and the original form of iron. The formulations tested were GlobiFer® Forte, a
combination of heme and non-heme iron containing 18 mg of elemental iron (hereinafter
referred to as nutraceutical product 1); GlobiFer®, a combination of heme and non-heme
iron containing 14 mg of elemental iron (hereinafter referred to as nutraceutical product
2); and a double dose of nutraceutical product 2. Using an in vitro 3D intestinal barrier
model, all three formulations significantly increased tight junction protein expression and
TEER values, indicating preserved barrier integrity. Iron absorption analysis revealed
that all three iron formulations had higher absorption rates than controls. Nutraceutical
product 1 showed the highest absorption, associated with increased expression of the iron
transporters such as the primary non-heme iron transporter, DMT1, and the leading apical
heme transporter, HCP-1. All three new formulations increased ferritin and ferroportin
levels, markers of systemic iron storage and regulation. Nutraceutical product 1 was found
to be the most effective, based on percentage. Overall, combining heme and non-heme
iron improved intestinal absorption and supported iron metabolism, with Nutraceutical
Product 1 proving the most promising in terms of efficacy and safety. These results support
the development of optimised dual-source iron supplements to improve bioavailability
and maintain intestinal barrier integrity, prerequisites for better efficacy and tolerability in
clinical use.
AB - Iron is essential for numerous physiological processes, including oxygen transport, energy
metabolism, and immune function. This study evaluated the efficacy and safety of three iron
formulations combining heme and non-heme iron, comparing them with existing market
products and the original form of iron. The formulations tested were GlobiFer® Forte, a
combination of heme and non-heme iron containing 18 mg of elemental iron (hereinafter
referred to as nutraceutical product 1); GlobiFer®, a combination of heme and non-heme
iron containing 14 mg of elemental iron (hereinafter referred to as nutraceutical product
2); and a double dose of nutraceutical product 2. Using an in vitro 3D intestinal barrier
model, all three formulations significantly increased tight junction protein expression and
TEER values, indicating preserved barrier integrity. Iron absorption analysis revealed
that all three iron formulations had higher absorption rates than controls. Nutraceutical
product 1 showed the highest absorption, associated with increased expression of the iron
transporters such as the primary non-heme iron transporter, DMT1, and the leading apical
heme transporter, HCP-1. All three new formulations increased ferritin and ferroportin
levels, markers of systemic iron storage and regulation. Nutraceutical product 1 was found
to be the most effective, based on percentage. Overall, combining heme and non-heme
iron improved intestinal absorption and supported iron metabolism, with Nutraceutical
Product 1 proving the most promising in terms of efficacy and safety. These results support
the development of optimised dual-source iron supplements to improve bioavailability
and maintain intestinal barrier integrity, prerequisites for better efficacy and tolerability in
clinical use.
KW - iron supplementation
KW - non-heme iron
KW - heme iron
KW - dual-source iron
KW - intestinal
absorption
KW - 3D in vitro intestinal barrier
KW - iron transporters
KW - iron supplementation
KW - non-heme iron
KW - heme iron
KW - dual-source iron
KW - intestinal
absorption
KW - 3D in vitro intestinal barrier
KW - iron transporters
UR - https://iris.uniupo.it/handle/11579/223462
U2 - 10.3390/biomedicines14010043
DO - 10.3390/biomedicines14010043
M3 - Article
SN - 2227-9059
VL - 14
JO - Biomedicines
JF - Biomedicines
IS - 1
ER -