Tulio Armando Lerma
Tulio Armando Lerma has a total of 44 co-authors. Here are the top co-authors by number of shared publications:
Manuel Palencia
33 shared publicationsJina M. Martínez
31 shared publicationsMayra A. Mora
Institución Universitaria Técnica para el Desarrollo Profesional
31 shared publicationsSixta L. Palencia
31 shared publicationsViviana Garcés
31 shared publications- Manuel Palencia
Research Group in Science with Technological Applications (GI-CAT), Department of Chemistry, Faculty of Natural and Exact Sciences, Universidad del Valle, Cali 760032, Colombia
23 shared publications
Latest Publications
- Open Access
- 6 May 2026
- Published by Universidad de Antioquia in Vitae
- Vol. 33 (2)
Sensory and physicochemical evaluation of specialty coffee formulations including lion’s mane mushroom (Hericium erinaceus)
BACKGROUND: Specialty coffee is widely consumed worldwide due to its energizing properties. However, there is a constant demand for innovations and improvements that mitigate the potential side effects of coffee through the inclusion of natural ingredients such as lion’s mane mushroom (Hericium erinaceus). Despite this, no studies have yet evaluated different formulations from both physicochemical and sensory perspectives. OBJECTIVE: To provide an initial approach to the formulation of a specialty coffee nutraceutical beverage including lion’s mane mushroom based on the physicochemical characterization and sensory evaluation of different formulations. METHODS: Two formulations were developed with different concentrations of lion’s mane (0.5 and 1.0 %), which were characterized physicochemically (soluble solids, titratable acidity, color, and pH) and evaluated through sensory analysis (fragrance/aroma, flavor, aftertaste, acidity, body, uniformity, sweetness, cup profile, and balance). RESULTS: The physicochemical results remained within the expected ranges for specialty coffee. Sensory evaluation showed that both formulations enriched with mushroom (0.5 % and 1.0 %) were well received by consumers. CONCLUSION: The 0.5 and 1.0 % Hericium erinaceus mushroom-enriched formulations in specialty coffee allow for a proper balance between the coffee’s flavor notes and the characteristics imparted by the mushroom.
- 6 May 2026
- Published by Universidad de Antioquia in Vitae
- Vol. 33 (2)
Open AccessSensory and physicochemical evaluation of specialty coffee formulations including lion’s mane mushroom (Hericium erinaceus)
BACKGROUND: Specialty coffee is widely consumed worldwide due to its energizing properties. However, there is a constant demand for innovations and improvements that mitigate the potential side effects of coffee through the inclusion of natural ingredients such as lion’s mane mushroom (Hericium erinaceus). Despite this, no studies have yet evaluated different formulations from both physicochemical and sensory perspectives. OBJECTIVE: To provide an initial approach to the formulation of a specialty coffee nutraceutical beverage including lion’s mane mushroom based on the physicochemical characterization and sensory evaluation of different formulations. METHODS: Two formulations were developed with different concentrations of lion’s mane (0.5 and 1.0 %), which were characterized physicochemically (soluble solids, titratable acidity, color, and pH) and evaluated through sensory analysis (fragrance/aroma, flavor, aftertaste, acidity, body, uniformity, sweetness, cup profile, and balance). RESULTS: The physicochemical results remained within the expected ranges for specialty coffee. Sensory evaluation showed that both formulations enriched with mushroom (0.5 % and 1.0 %) were well received by consumers. CONCLUSION: The 0.5 and 1.0 % Hericium erinaceus mushroom-enriched formulations in specialty coffee allow for a proper balance between the coffee’s flavor notes and the characteristics imparted by the mushroom.
- Open Access
Organoclay Microparticle-Enhanced Microfiltration for the Removal of Acid Red 27 in Aqueous Systems
The microparticle-enhanced microfiltration is a technique that combines the use of microparticulate adsorbent material dispersed in aqueous solution and microfiltration membranes for the removal of ions and emerging contaminants with low energy consumption. Thus, the objective of this work was to synthesize an organoclay, BAPTES, based on bentonite and (3-aminopropyl)triethoxysilane for use as a semi-synthetic adsorbent material in the microparticle-enhanced microfiltration process for the removal of AR27 in aqueous systems. For this purpose, the obtained organoclay was structurally characterized by FTIR-ATR-FEDS, SEM-EDS, DLS, and thermal analysis. In addition, equilibrium adsorption and kinetic studies of AR27 were performed. The results showed a significant increase in the adsorption capacity of AR27 by organoclay (86.06%) compared to natural bentonite (2.10%), due to the presence of ionizable amino groups in the organoclay structure that promote electrostatic interactions with the dye. Furthermore, kinetic studies showed that the adsorption process follows a pseudo-first-order model and that the equilibrium data better fits the Temkin model, indicating a heterogeneous adsorption surface with different binding energies. The evaluation of enhanced microfiltration with BAPTES microparticles showed that the adsorption capacity obtained in continuous flow experiments (14.25–33.63 mg g−1) was lower than that determined experimentally under equilibrium conditions (~39.5 mg g−1), suggesting that the residence time of the analyte and the adsorbent in the filtration cell is a determining factor in the retention values obtained. In addition, desorption studies revealed that basic pH had a greater effect than the presence of salts and the use of ethanol, favoring the weakening of the AR27-BAPTES interaction. Finally, the results highlight the potential use of BAPTES microparticle-enhanced microfiltration in applications involving the treatment of contaminated industrial effluents.
Open AccessOrganoclay Microparticle-Enhanced Microfiltration for the Removal of Acid Red 27 in Aqueous Systems
The microparticle-enhanced microfiltration is a technique that combines the use of microparticulate adsorbent material dispersed in aqueous solution and microfiltration membranes for the removal of ions and emerging contaminants with low energy consumption. Thus, the objective of this work was to synthesize an organoclay, BAPTES, based on bentonite and (3-aminopropyl)triethoxysilane for use as a semi-synthetic adsorbent material in the microparticle-enhanced microfiltration process for the removal of AR27 in aqueous systems. For this purpose, the obtained organoclay was structurally characterized by FTIR-ATR-FEDS, SEM-EDS, DLS, and thermal analysis. In addition, equilibrium adsorption and kinetic studies of AR27 were performed. The results showed a significant increase in the adsorption capacity of AR27 by organoclay (86.06%) compared to natural bentonite (2.10%), due to the presence of ionizable amino groups in the organoclay structure that promote electrostatic interactions with the dye. Furthermore, kinetic studies showed that the adsorption process follows a pseudo-first-order model and that the equilibrium data better fits the Temkin model, indicating a heterogeneous adsorption surface with different binding energies. The evaluation of enhanced microfiltration with BAPTES microparticles showed that the adsorption capacity obtained in continuous flow experiments (14.25–33.63 mg g−1) was lower than that determined experimentally under equilibrium conditions (~39.5 mg g−1), suggesting that the residence time of the analyte and the adsorbent in the filtration cell is a determining factor in the retention values obtained. In addition, desorption studies revealed that basic pH had a greater effect than the presence of salts and the use of ethanol, favoring the weakening of the AR27-BAPTES interaction. Finally, the results highlight the potential use of BAPTES microparticle-enhanced microfiltration in applications involving the treatment of contaminated industrial effluents.
- Top Cited PapersOpen Access
Physicochemical Characterization and Properties of Cassava Starch: A Review
Cassava (Manihot esculenta Crantz) is a tuber and one of the most important sources of commercial production in the world, with high consumed food produced in the tropics contributing to high quantity of calories to the diet. The principal component of the cassava root is starch, a polysaccharide composed of amylose and amylopectin, where the physicochemical property of the biopolymer is altered in different cooking processes. This review summarizes and provides information about cassava starch structure, morphology, and physicochemical properties, such as gelatinization, pasting, and retrogradation of cassava starch, as well as the use of methods of characterization to follow and analyze the physical and chemical changes of cassava starch.
Top Cited PapersOpen AccessPhysicochemical Characterization and Properties of Cassava Starch: A Review
Cassava (Manihot esculenta Crantz) is a tuber and one of the most important sources of commercial production in the world, with high consumed food produced in the tropics contributing to high quantity of calories to the diet. The principal component of the cassava root is starch, a polysaccharide composed of amylose and amylopectin, where the physicochemical property of the biopolymer is altered in different cooking processes. This review summarizes and provides information about cassava starch structure, morphology, and physicochemical properties, such as gelatinization, pasting, and retrogradation of cassava starch, as well as the use of methods of characterization to follow and analyze the physical and chemical changes of cassava starch.
- Open Access
CTAB Surfactant Promotes Rapid, Efficient, and Simultaneous Removal of Cationic and Anionic Dyes through Adsorption on Glycerol/Citrate Polyester
The discharge of dye waste by industries has caused environmental impacts on water properties, aquatic species, and human life. The production of eco-friendly materials for dye removal from wastewater has gained increasing interest, particularly through adsorption, as it is an efficient method for removing pollutants. However, the selectivity and limited adsorption capacity of materials for simultaneously adsorbing cationic and anionic dyes make it challenging to address the prevailing dye effluent issue. In this work, a poly(glycerol citrate) polyester was prepared without a solvent, using microwave heating, and was combined with cetyltrimethylammonium bromide (CTAB) to modulate the simultaneous adsorption of cationic (Rhodamine B, RB) and anionic dyes (acid blue 113, AB and acid red 27, AR). The formation of the polyester was successfully confirmed by ATR-FTIR and the thermal properties were evaluated by TGA and DCS. In the presence of CTAB 5 mM, the material removes almost 100% of the dyes, reaching the kinetics equilibrium in 30 min following the Pseudo-second order model. Additionally, dye adsorption on the polyester in the presence of CTAB was described by the Freundlich isotherm model, indicating a heterogeneous polyester surface that promotes a multi-layer adsorption driven by electrostatic interaction and hydrogen bonds. The material showed an adsorption capacity of 73.7 ± 3.2, 82.1 ± 4.4, and 21.2 ± 0.6 mg/g for RB, AB, and AR, respectively. Our results provide evidence that the poly(glycerol citrate)/CTAB has a higher potential for application in wastewater treatment to remove both anionic and cationic dyes.
Open AccessCTAB Surfactant Promotes Rapid, Efficient, and Simultaneous Removal of Cationic and Anionic Dyes through Adsorption on Glycerol/Citrate Polyester
The discharge of dye waste by industries has caused environmental impacts on water properties, aquatic species, and human life. The production of eco-friendly materials for dye removal from wastewater has gained increasing interest, particularly through adsorption, as it is an efficient method for removing pollutants. However, the selectivity and limited adsorption capacity of materials for simultaneously adsorbing cationic and anionic dyes make it challenging to address the prevailing dye effluent issue. In this work, a poly(glycerol citrate) polyester was prepared without a solvent, using microwave heating, and was combined with cetyltrimethylammonium bromide (CTAB) to modulate the simultaneous adsorption of cationic (Rhodamine B, RB) and anionic dyes (acid blue 113, AB and acid red 27, AR). The formation of the polyester was successfully confirmed by ATR-FTIR and the thermal properties were evaluated by TGA and DCS. In the presence of CTAB 5 mM, the material removes almost 100% of the dyes, reaching the kinetics equilibrium in 30 min following the Pseudo-second order model. Additionally, dye adsorption on the polyester in the presence of CTAB was described by the Freundlich isotherm model, indicating a heterogeneous polyester surface that promotes a multi-layer adsorption driven by electrostatic interaction and hydrogen bonds. The material showed an adsorption capacity of 73.7 ± 3.2, 82.1 ± 4.4, and 21.2 ± 0.6 mg/g for RB, AB, and AR, respectively. Our results provide evidence that the poly(glycerol citrate)/CTAB has a higher potential for application in wastewater treatment to remove both anionic and cationic dyes.
- Open Access
Synthesis and Characterization of Nanocomposite Hydrogels Based on Poly(Sodium 4-Styrene Sulfonate) under Very-High Concentration Regimen of Clays (Bentonite and Kaolinite)
The aim of this work was to synthesize and study the functional properties of polymer-clay nanocomposite (PCNCs) based on poly(sodium 4-styrene sulfonate) (NaPSS) and two types of clay in the dispersed phase: bentonite and kaolinite, in order to advance in the development of new geomimetic materials for agricultural and environmental applications. In this study, the effect of adding high concentrations of clay (10–20 wt. %) on the structural and functional properties of a polymer–clay nanocomposite was evaluated. The characterization by infrared spectroscopy made it possible to show that the PCNCs had a hybrid nature structure through the identification of typical vibration bands of the clay matrix and NaPSS. In addition, scanning electron microscopy allowed us to verify its hybrid composition and an amorphous particle-like morphology. The thermal characterization showed degradation temperatures higher than ~300 °C with Tg values higher than 100 °C and variables depending on the clay contents. In addition, the PCNCs showed a high water-retention capacity (>2900%) and cation exchange capacity (>112 meq/100 g). Finally, the results demonstrated the ability of geomimetic conditioners to mimic the structure and functional properties of soils, suggesting their potential application in improving soil quality for plant growth.
Open AccessSynthesis and Characterization of Nanocomposite Hydrogels Based on Poly(Sodium 4-Styrene Sulfonate) under Very-High Concentration Regimen of Clays (Bentonite and Kaolinite)
The aim of this work was to synthesize and study the functional properties of polymer-clay nanocomposite (PCNCs) based on poly(sodium 4-styrene sulfonate) (NaPSS) and two types of clay in the dispersed phase: bentonite and kaolinite, in order to advance in the development of new geomimetic materials for agricultural and environmental applications. In this study, the effect of adding high concentrations of clay (10–20 wt. %) on the structural and functional properties of a polymer–clay nanocomposite was evaluated. The characterization by infrared spectroscopy made it possible to show that the PCNCs had a hybrid nature structure through the identification of typical vibration bands of the clay matrix and NaPSS. In addition, scanning electron microscopy allowed us to verify its hybrid composition and an amorphous particle-like morphology. The thermal characterization showed degradation temperatures higher than ~300 °C with Tg values higher than 100 °C and variables depending on the clay contents. In addition, the PCNCs showed a high water-retention capacity (>2900%) and cation exchange capacity (>112 meq/100 g). Finally, the results demonstrated the ability of geomimetic conditioners to mimic the structure and functional properties of soils, suggesting their potential application in improving soil quality for plant growth.
- Open Access
Nanocarrier of α-Tocopheryl Succinate Based on a Copolymer Derivative of (4,7-dichloroquinolin-2-yl)methanol and Its Cytotoxicity against a Breast Cancer Cell Line
In order to improve the water solubility and, therefore, bioavailability and therapeutic activity of anticancer hydrophobic drug α-tocopherol succinate (α-TOS), in this work, copolymers were synthesized via free radicals from QMES (1-[4,7-dichloroquinolin-2-ylmethyl]-4-methacryloyloxyethyl succinate) and VP (N-vinyl-2-pirrolidone) using different molar ratios, and were used to nanoencapsulate and deliver α-TOS into cancer cells MCF-7. QMES monomer was chosen because the QMES pendant group in the polymer tends to hydrolyze to form free 4,7-dichloro-2-quinolinemethanol (QOH), which also, like α-TOS, exhibit anti-proliferative effects on cancerous cells. From the QMES-VP 30:70 (QMES-30) and 40:60 (QMES-40) copolymers obtained, it was possible to prepare aqueous suspensions of empty nanoparticles (NPs) loaded with α-TOS by nanoprecipitation. The diameter and encapsulation efficiency (%EE) of the QMES-30 NPs loaded with α-TOS were 128.6 nm and 52%; while for the QMES-40 NPs loaded with α-TOS, they were 148.8 nm and 65%. The results of the AlamarBlue assay at 72 h of treatment show that empty QMES-30 NPs (without α-TOS) produced a marked cytotoxic effect on MCF-7 breast cancer cells, corresponding to an IC50 value of 0.043 mg mL−1, and importantly, they did not exhibit cytotoxicity against healthy HUVEC cells. Furthermore, NP-QMES-40 loaded with α-TOS were cytotoxic with an IC50 value of 0.076 mg mL−1, demonstrating a progressive release of α-TOS; however, the latter nanoparticles were also cytotoxic to healthy cells in the range of the assayed concentrations. These results contribute to the search for a new polymeric nanocarrier of QOH, α-TOS or other hydrophobic drugs for the treatment of cancer or others diseases treatable with these drugs.
Open AccessNanocarrier of α-Tocopheryl Succinate Based on a Copolymer Derivative of (4,7-dichloroquinolin-2-yl)methanol and Its Cytotoxicity against a Breast Cancer Cell Line
In order to improve the water solubility and, therefore, bioavailability and therapeutic activity of anticancer hydrophobic drug α-tocopherol succinate (α-TOS), in this work, copolymers were synthesized via free radicals from QMES (1-[4,7-dichloroquinolin-2-ylmethyl]-4-methacryloyloxyethyl succinate) and VP (N-vinyl-2-pirrolidone) using different molar ratios, and were used to nanoencapsulate and deliver α-TOS into cancer cells MCF-7. QMES monomer was chosen because the QMES pendant group in the polymer tends to hydrolyze to form free 4,7-dichloro-2-quinolinemethanol (QOH), which also, like α-TOS, exhibit anti-proliferative effects on cancerous cells. From the QMES-VP 30:70 (QMES-30) and 40:60 (QMES-40) copolymers obtained, it was possible to prepare aqueous suspensions of empty nanoparticles (NPs) loaded with α-TOS by nanoprecipitation. The diameter and encapsulation efficiency (%EE) of the QMES-30 NPs loaded with α-TOS were 128.6 nm and 52%; while for the QMES-40 NPs loaded with α-TOS, they were 148.8 nm and 65%. The results of the AlamarBlue assay at 72 h of treatment show that empty QMES-30 NPs (without α-TOS) produced a marked cytotoxic effect on MCF-7 breast cancer cells, corresponding to an IC50 value of 0.043 mg mL−1, and importantly, they did not exhibit cytotoxicity against healthy HUVEC cells. Furthermore, NP-QMES-40 loaded with α-TOS were cytotoxic with an IC50 value of 0.076 mg mL−1, demonstrating a progressive release of α-TOS; however, the latter nanoparticles were also cytotoxic to healthy cells in the range of the assayed concentrations. These results contribute to the search for a new polymeric nanocarrier of QOH, α-TOS or other hydrophobic drugs for the treatment of cancer or others diseases treatable with these drugs.
- 26 April 2023
- Published by Springer Nature
- p. 1937-1959
Modulation of the Bioactivity of Inorganic Nanomaterials by Controlling Nanobiointerface
- 26 April 2023
- Published by Springer Nature
- p. 1937-1959
Modulation of the Bioactivity of Inorganic Nanomaterials by Controlling Nanobiointerface
- 29 November 2022
- Published by Springer Nature
- p. 1-23
Modulation of the Bioactivity of Inorganic Nanomaterials by Controlling Nanobiointerface
- 29 November 2022
- Published by Springer Nature
- p. 1-23
Modulation of the Bioactivity of Inorganic Nanomaterials by Controlling Nanobiointerface
- 2 November 2022
- Published by Springer Nature in Journal of Polymer Research
- Vol. 29 (11) , 1-15
Novel one-pot synthesis of polymeric hydrogels based on isocyanate click chemistry: Structural and functional characterization
- 2 November 2022
- Published by Springer Nature in Journal of Polymer Research
- Vol. 29 (11) , 1-15
Novel one-pot synthesis of polymeric hydrogels based on isocyanate click chemistry: Structural and functional characterization